Recent Advances in the Study of In Situ Combustion for Enhanced Oil Recovery
Abstract
:1. Introduction
2. Prior History of the In Situ Combustion Method
3. Scientometric Analysis of Research Activities
4. The Main Processes of the In Situ Combustion Method
5. Basic In Situ Combustion Technologies
6. Recent Advances in the Study of In Situ Combustion Methods
6.1. Review of Experimental Approaches into the Study of the In Situ Combustion Method
6.2. Review of Numerical Studies of In Situ Fuel Combustion Implementation Technologies
- Coke formation
- Combustion of heavy oil fraction
- Combustion of light oil fraction
- Combustion of coke
7. Conclusions
- The development of the classic in situ combustion method has led to its new modifications that differ from each other both structurally and in their basic approaches to forming the combustion front. Unfortunately, none of four implemented technologies (ND-ISC, THAITM, COSH, and CAGD) has seen widespread use due to the lack of an evidence base for their successful application in the field.
- The main studies of the in situ combustion method are associated with laboratory and experimental works, as well as numerical simulation. The laboratory works mainly determine the effects of the oil-source rock on the combustion processes, because clay components of the rocks can form the basis of new series of catalysts to mitigate the conditions of in situ combustion. It was proven that clays containing quartz and kaolinite, montmorillonite, mica, and clinochlore, as well as the presence of calcite and dolomite, exhibit a good catalytic effect. The development of soluble catalysts is currently under active consideration. For example, copper stearate demonstrates a good catalytic effect, shifting the combustion reaction to a lower temperature range.
- Experimental studies have thus far been aimed at obtaining data on oil reactivity, determining the ignition conditions by revealing the nature of raw hydrocarbons, and most importantly, determining its combustion characteristics. As a rule, these obtained kinetic parameters have been used as basic data for numerical simulation. It is the experimental combustion in a cell that allows us to determine the amount of fuel needed for cracking, as well as estimate the combustion front propagation rate. The main difficulties in conducting experimental studies are associated with the lack of acceptable criteria for planning experiments; therefore, a numerical simulation of the process is used as an alternative method. Different combinations of chemical reactions lead to a variety of numerical models. One of the most common is a scheme of reactions, which includes pyrolysis and combustion; at the same time, the inorganic decomposition process is unpopular since its activation requires high temperatures.
- To implement the method, it is necessary to solve the problems of initiating the exothermic reaction center, as well as for maintaining the optimal temperature, stability, and integrity of temperature and chemical fronts in the reservoir. However, the main problem is the unstable combustion propagation, especially if the reservoir structure is heterogeneous. A difference between the viscosity of the injected air and the reservoir saturating fluids leads to air filtration in the most permeable areas. This results in a decrease in the efficiency of in situ combustion, making its implementation quite dangerous. In addition, during the implementation of in situ combustion in the oil fields containing heavy high-viscosity oil, an excessive amount of coke is often formed, which is necessary to maintain combustion. This increases specific air consumption and decreases the combustion front propagation rate. Another problem is the reduced coke-forming ability of oils in fields containing light low-viscosity oil, which leads to a loss of the combustion front as it moves deeper into the formation. These problems should be solved using detailed numerical simulation with experimental verification of the main elements of the model.
Author Contributions
Funding
Data Availability Statement
Conflicts of Interest
Nomenclature
CAGD | Combustion assisted gravity drainage |
COSH | Combustion override split-production horizontal-well |
Da | Damköhler number |
ES-SAGD | Expanding Solvent SAGD |
EHO | Extra heavy oil |
H/C | Ratio between the carbon and hydrogen atoms |
HTO | High temperature oxidation |
HO | Heavy oil |
ISC | In situ combustion |
LO | Light oil |
LTC | Low-temperature combustion |
LTO | Low temperature oxidation |
ONGC | Oil and Natural Corporation |
PMTEC | Porous medium thermo-effect cell |
PRMS | Petroleum resource management system |
RLF | Reaction-leading front |
RTF | Reaction-trailing front |
SAP | Solvent aided process |
SAGD | Steam-assisted gravity drainage |
SAS | Steam alternating solvent |
TD-ISC | Top-down in situ combustion |
THAI | Toe-to-heel air injection |
VAPEX | Vapor extraction |
VKC | Virtual kinetic cell |
WOS | Web of Science |
Water/air consumption, m3/s | |
Model reaction rate | |
Prototype speed | |
φ | Medium porosity |
Mass source term in, kg/m3 | |
Density and velocity of the gas mixture | |
Oil density | |
Effective heat conductivity | |
Specific heat capacity of oil shale and i gas phase, respectively | |
Q | Heat source term in equation due to chemical reactions |
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Artificial Ignition Method | Advantages | Disadvantages |
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Gas burners |
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Catalytic heaters |
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Chemical ignition |
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Steam injection |
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Name | Approaches | |||||
---|---|---|---|---|---|---|
*1 | *2 | *3 | *4 | *5 | *6 | |
Capillary forces | ✓ | - | - | - | ||
✓ | ± | ✓ | ✓ | ✓ | ✓ | |
Diffusion forces | ✓ | ✓ (one direction only) | ✓ | ✓ | ✓ | ✓ |
Mass transfer to viscosity ratio | ||||||
Reaction rate | - | - | ✓ | ✓ | - | ✓ |
Gravity forces | - | ✓ | ✓ | ✓ | ✓ | ✓ |
Dispersion forces | - | ✓ | ✓ | ✓ | - | ✓ |
Gravity forces to viscosity | - | - | - | ✓ | ✓ | ✓ |
Dispersed effect | three-dimensional | one-dimensional for the combustion pipe | scattering effect | |||
model reaction rate prototype speed |
Composition of the Catalyst | Effect | Results |
---|---|---|
1. Clay mixtures of 3 wt% | Catalytic | Controls the combustion front |
2. Quartz and mica containing clay | Catalytic | Mica leads to a decrease in activation energy |
3. Clinochlor and talc containing clay | Inhibitory | Leads to a delay in the reaction of isomerization and decomposition, as well as in the reaction of oxidative cracking |
4. Kaolinite, montmorillonite, mica, and clinochlor containing clay | Catalytic | Controls the combustion front, but does not lead to a shift at the stage of high-temperature oxidation |
5. The level of calcite and dolomite | Catalytic | Provides light ignition and significantly reduces the activation energy |
6. Copper stearate | Catalytic | Shifts the combustion reactions to a lower temperature range, especially during high-temperature oxidation. Increases the efficiency of coke combustion. |
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Minakov, A.V.; Meshkova, V.D.; Guzey, D.V.; Pryazhnikov, M.I. Recent Advances in the Study of In Situ Combustion for Enhanced Oil Recovery. Energies 2023, 16, 4266. https://doi.org/10.3390/en16114266
Minakov AV, Meshkova VD, Guzey DV, Pryazhnikov MI. Recent Advances in the Study of In Situ Combustion for Enhanced Oil Recovery. Energies. 2023; 16(11):4266. https://doi.org/10.3390/en16114266
Chicago/Turabian StyleMinakov, Andrey V., Victoria D. Meshkova, Dmitry Viktorovich Guzey, and Maksim I. Pryazhnikov. 2023. "Recent Advances in the Study of In Situ Combustion for Enhanced Oil Recovery" Energies 16, no. 11: 4266. https://doi.org/10.3390/en16114266
APA StyleMinakov, A. V., Meshkova, V. D., Guzey, D. V., & Pryazhnikov, M. I. (2023). Recent Advances in the Study of In Situ Combustion for Enhanced Oil Recovery. Energies, 16(11), 4266. https://doi.org/10.3390/en16114266