CA2897402C - Use of foam with in situ combustion process - Google Patents
Use of foam with in situ combustion process Download PDFInfo
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- CA2897402C CA2897402C CA2897402A CA2897402A CA2897402C CA 2897402 C CA2897402 C CA 2897402C CA 2897402 A CA2897402 A CA 2897402A CA 2897402 A CA2897402 A CA 2897402A CA 2897402 C CA2897402 C CA 2897402C
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- water
- oil
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- oxygen
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- 238000002485 combustion reaction Methods 0.000 title claims abstract description 59
- 239000006260 foam Substances 0.000 title claims abstract description 44
- 238000011065 in-situ storage Methods 0.000 title claims abstract description 28
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 72
- 238000000034 method Methods 0.000 claims abstract description 62
- 238000011084 recovery Methods 0.000 claims abstract description 10
- 239000007789 gas Substances 0.000 claims description 64
- 239000007924 injection Substances 0.000 claims description 30
- 238000002347 injection Methods 0.000 claims description 30
- 239000001301 oxygen Substances 0.000 claims description 30
- 229910052760 oxygen Inorganic materials 0.000 claims description 30
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 28
- 238000004519 manufacturing process Methods 0.000 claims description 25
- 239000011435 rock Substances 0.000 claims description 22
- 239000012530 fluid Substances 0.000 claims description 17
- 230000015572 biosynthetic process Effects 0.000 claims description 14
- 229930195733 hydrocarbon Natural products 0.000 claims description 12
- 150000002430 hydrocarbons Chemical class 0.000 claims description 12
- 238000010796 Steam-assisted gravity drainage Methods 0.000 claims description 11
- 239000003795 chemical substances by application Substances 0.000 claims description 10
- 239000000443 aerosol Substances 0.000 claims description 8
- 239000000839 emulsion Substances 0.000 claims description 8
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 claims description 8
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 claims description 6
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 claims description 6
- 239000003513 alkali Substances 0.000 claims description 6
- 230000002000 scavenging effect Effects 0.000 claims description 6
- 239000004094 surface-active agent Substances 0.000 claims description 6
- -1 aromatic sulfonates Chemical class 0.000 claims description 5
- 239000012267 brine Substances 0.000 claims description 5
- 238000001246 colloidal dispersion Methods 0.000 claims description 5
- HPALAKNZSZLMCH-UHFFFAOYSA-M sodium;chloride;hydrate Chemical compound O.[Na+].[Cl-] HPALAKNZSZLMCH-UHFFFAOYSA-M 0.000 claims description 5
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 4
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 claims description 4
- UGFAIRIUMAVXCW-UHFFFAOYSA-N Carbon monoxide Chemical compound [O+]#[C-] UGFAIRIUMAVXCW-UHFFFAOYSA-N 0.000 claims description 4
- ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 claims description 4
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 claims description 4
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 claims description 4
- 238000009841 combustion method Methods 0.000 claims description 3
- 150000003839 salts Chemical class 0.000 claims description 3
- RWSOTUBLDIXVET-UHFFFAOYSA-N Dihydrogen sulfide Chemical compound S RWSOTUBLDIXVET-UHFFFAOYSA-N 0.000 claims description 2
- UIIMBOGNXHQVGW-DEQYMQKBSA-M Sodium bicarbonate-14C Chemical compound [Na+].O[14C]([O-])=O UIIMBOGNXHQVGW-DEQYMQKBSA-M 0.000 claims description 2
- 239000003570 air Substances 0.000 claims description 2
- 150000001336 alkenes Chemical class 0.000 claims description 2
- 150000008055 alkyl aryl sulfonates Chemical class 0.000 claims description 2
- 150000004996 alkyl benzenes Chemical class 0.000 claims description 2
- 239000001273 butane Substances 0.000 claims description 2
- 229910000019 calcium carbonate Inorganic materials 0.000 claims description 2
- UBAZGMLMVVQSCD-UHFFFAOYSA-N carbon dioxide;molecular oxygen Chemical compound O=O.O=C=O UBAZGMLMVVQSCD-UHFFFAOYSA-N 0.000 claims description 2
- 229910002091 carbon monoxide Inorganic materials 0.000 claims description 2
- 239000003546 flue gas Substances 0.000 claims description 2
- 239000001257 hydrogen Substances 0.000 claims description 2
- 229910052739 hydrogen Inorganic materials 0.000 claims description 2
- 125000004435 hydrogen atom Chemical class [H]* 0.000 claims description 2
- 229910000037 hydrogen sulfide Inorganic materials 0.000 claims description 2
- ZLNQQNXFFQJAID-UHFFFAOYSA-L magnesium carbonate Chemical compound [Mg+2].[O-]C([O-])=O ZLNQQNXFFQJAID-UHFFFAOYSA-L 0.000 claims description 2
- 239000001095 magnesium carbonate Substances 0.000 claims description 2
- 229910000021 magnesium carbonate Inorganic materials 0.000 claims description 2
- IJDNQMDRQITEOD-UHFFFAOYSA-N n-butane Chemical compound CCCC IJDNQMDRQITEOD-UHFFFAOYSA-N 0.000 claims description 2
- OFBQJSOFQDEBGM-UHFFFAOYSA-N n-pentane Natural products CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 claims description 2
- 239000003345 natural gas Substances 0.000 claims description 2
- 229910052757 nitrogen Inorganic materials 0.000 claims description 2
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 claims description 2
- 239000011736 potassium bicarbonate Substances 0.000 claims description 2
- 229910000028 potassium bicarbonate Inorganic materials 0.000 claims description 2
- 235000015497 potassium bicarbonate Nutrition 0.000 claims description 2
- 229910000027 potassium carbonate Inorganic materials 0.000 claims description 2
- 235000011181 potassium carbonates Nutrition 0.000 claims description 2
- TYJJADVDDVDEDZ-UHFFFAOYSA-M potassium hydrogencarbonate Chemical compound [K+].OC([O-])=O TYJJADVDDVDEDZ-UHFFFAOYSA-M 0.000 claims description 2
- 239000001294 propane Substances 0.000 claims description 2
- 239000013535 sea water Substances 0.000 claims description 2
- 229910000029 sodium carbonate Inorganic materials 0.000 claims description 2
- 150000003871 sulfonates Chemical class 0.000 claims description 2
- 239000004088 foaming agent Substances 0.000 abstract description 29
- 238000000926 separation method Methods 0.000 abstract description 6
- 238000002156 mixing Methods 0.000 abstract description 3
- 239000000084 colloidal system Substances 0.000 abstract description 2
- 239000003921 oil Substances 0.000 description 64
- 230000008569 process Effects 0.000 description 12
- 239000010426 asphalt Substances 0.000 description 5
- 239000000295 fuel oil Substances 0.000 description 5
- 239000008131 herbal destillate Substances 0.000 description 5
- 238000010794 Cyclic Steam Stimulation Methods 0.000 description 4
- 239000010779 crude oil Substances 0.000 description 4
- 230000035699 permeability Effects 0.000 description 4
- MYMOFIZGZYHOMD-UHFFFAOYSA-N Dioxygen Chemical compound O=O MYMOFIZGZYHOMD-UHFFFAOYSA-N 0.000 description 3
- 230000007423 decrease Effects 0.000 description 3
- 229910001882 dioxygen Inorganic materials 0.000 description 3
- 239000006185 dispersion Substances 0.000 description 3
- 238000005516 engineering process Methods 0.000 description 3
- 239000000446 fuel Substances 0.000 description 3
- 230000005484 gravity Effects 0.000 description 3
- 239000007788 liquid Substances 0.000 description 3
- 239000003208 petroleum Substances 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- 239000000654 additive Substances 0.000 description 2
- 230000000996 additive effect Effects 0.000 description 2
- 239000002280 amphoteric surfactant Substances 0.000 description 2
- 239000002585 base Substances 0.000 description 2
- 125000002091 cationic group Chemical group 0.000 description 2
- 150000001875 compounds Chemical class 0.000 description 2
- 230000006835 compression Effects 0.000 description 2
- 238000007906 compression Methods 0.000 description 2
- 238000000605 extraction Methods 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 230000003993 interaction Effects 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 238000005259 measurement Methods 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 230000001483 mobilizing effect Effects 0.000 description 2
- 238000010791 quenching Methods 0.000 description 2
- BVKZGUZCCUSVTD-UHFFFAOYSA-M Bicarbonate Chemical class OC([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-M 0.000 description 1
- 239000004215 Carbon black (E152) Substances 0.000 description 1
- 241000237858 Gastropoda Species 0.000 description 1
- XQCFHQBGMWUEMY-ZPUQHVIOSA-N Nitrovin Chemical compound C=1C=C([N+]([O-])=O)OC=1\C=C\C(=NNC(=N)N)\C=C\C1=CC=C([N+]([O-])=O)O1 XQCFHQBGMWUEMY-ZPUQHVIOSA-N 0.000 description 1
- CBENFWSGALASAD-UHFFFAOYSA-N Ozone Chemical compound [O-][O+]=O CBENFWSGALASAD-UHFFFAOYSA-N 0.000 description 1
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 1
- 238000010793 Steam injection (oil industry) Methods 0.000 description 1
- 238000010797 Vapor Assisted Petroleum Extraction Methods 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- 125000000129 anionic group Chemical group 0.000 description 1
- 230000008901 benefit Effects 0.000 description 1
- 230000000903 blocking effect Effects 0.000 description 1
- 150000004649 carbonic acid derivatives Chemical class 0.000 description 1
- 239000003093 cationic surfactant Substances 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- 239000000567 combustion gas Substances 0.000 description 1
- 238000009833 condensation Methods 0.000 description 1
- 230000005494 condensation Effects 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 230000001419 dependent effect Effects 0.000 description 1
- 238000006073 displacement reaction Methods 0.000 description 1
- 238000005553 drilling Methods 0.000 description 1
- 238000005187 foaming Methods 0.000 description 1
- 239000013505 freshwater Substances 0.000 description 1
- 239000005431 greenhouse gas Substances 0.000 description 1
- 150000004679 hydroxides Chemical class 0.000 description 1
- 150000002500 ions Chemical class 0.000 description 1
- 239000000155 melt Substances 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 230000000813 microbial effect Effects 0.000 description 1
- 235000013379 molasses Nutrition 0.000 description 1
- 239000002736 nonionic surfactant Substances 0.000 description 1
- 230000001590 oxidative effect Effects 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 230000000737 periodic effect Effects 0.000 description 1
- 229910052698 phosphorus Inorganic materials 0.000 description 1
- 239000011574 phosphorus Substances 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 238000011176 pooling Methods 0.000 description 1
- 238000001556 precipitation Methods 0.000 description 1
- 230000002265 prevention Effects 0.000 description 1
- 230000000171 quenching effect Effects 0.000 description 1
- 238000007670 refining Methods 0.000 description 1
- 239000004576 sand Substances 0.000 description 1
- XZPVPNZTYPUODG-UHFFFAOYSA-M sodium;chloride;dihydrate Chemical group O.O.[Na+].[Cl-] XZPVPNZTYPUODG-UHFFFAOYSA-M 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 238000001179 sorption measurement Methods 0.000 description 1
- 230000002269 spontaneous effect Effects 0.000 description 1
- 230000003068 static effect Effects 0.000 description 1
- 239000002352 surface water Substances 0.000 description 1
- 239000002888 zwitterionic surfactant Substances 0.000 description 1
Classifications
-
- E—FIXED CONSTRUCTIONS
- E21—EARTH DRILLING; MINING
- E21B—EARTH DRILLING, e.g. DEEP DRILLING; OBTAINING OIL, GAS, WATER, SOLUBLE OR MELTABLE MATERIALS OR A SLURRY OF MINERALS FROM WELLS
- E21B43/00—Methods or apparatus for obtaining oil, gas, water, soluble or meltable materials or a slurry of minerals from wells
- E21B43/16—Enhanced recovery methods for obtaining hydrocarbons
- E21B43/166—Injecting a gaseous medium; Injecting a gaseous medium and a liquid medium
-
- E—FIXED CONSTRUCTIONS
- E21—EARTH DRILLING; MINING
- E21B—EARTH DRILLING, e.g. DEEP DRILLING; OBTAINING OIL, GAS, WATER, SOLUBLE OR MELTABLE MATERIALS OR A SLURRY OF MINERALS FROM WELLS
- E21B43/00—Methods or apparatus for obtaining oil, gas, water, soluble or meltable materials or a slurry of minerals from wells
- E21B43/16—Enhanced recovery methods for obtaining hydrocarbons
- E21B43/24—Enhanced recovery methods for obtaining hydrocarbons using heat, e.g. steam injection
- E21B43/243—Combustion in situ
Abstract
The present invention relates to a novel method of maintaining a steady and/or proper water-gas ratio for the wet in situ combustion process for oil recovery. In particular, the method comprises mixing water with a foaming agent, or some other colloid capable of generating foam, in addition to gas. The foam carries the water through heated reservoirs more efficiently and prevents separation from the gas. As such, more heat can be scavenged, thus an increased amount of steam is generated and transferred to the oil to increase its recovery.
Description
USE OF FOAM WITH IN SITU COMBUSTION PROCESS
FIELD OF THE INVENTION
[0003] The invention relates to methods of improving the effectiveness of wet in situ combustion (ISC) processes to accelerate oil production and particularly to an improved wet in situ combustion process utilizing foam. Water containing a foaming agent is injected along with an oxygen-containing gas to maintain a consistent water-gas ratio, to facilitate water-reservoir rock contact and to prevent separation of water and gas.
BACKGROUND OF THE INVENTION
[0004] Conventional oil reserves are preferred sources of oil because they provide a high ratio of extracted energy over energy used in regards to the extraction and refining processes it undergoes. Unfortunately, due to the physics of fluid flow, not all conventional oil can be produced. Additionally, as conventional oil sources become scarce or economically non-viable due to depletion, unconventional oil sources are becoming a potential supply of oil. But, unconventional oil production is also problematic because it consists of extra heavy oils having a consistency ranging from that of heavy molasses to a solid at room temperature and may also be located in the reservoir rocks. These properties make it difficult to simply pump the oil out of the ground; thus, its production is a less efficient process than conventional oil.
[0005] As a result, enhanced oil recovery (EOR) techniques are often employed to increase the amount of subterranean crude oil extracted. Using EOR, 30-60% or more of the original oil can be extracted. Additionally, EOR finds applications in both conventional and unconventional oil reserves.
[0006] During EOR, compounds not naturally found in the reservoir are injected into the reservoir in a well other than the producing well to assist in oil recovery.
Simply stated, EOR
techniques overcome the physical forces holding the oil hydrocarbons underground. There are many types of EOR techniques that are categorized by the compound being injection: gas injection, chemical injection, microbial injection or thermal recovery. While there are many types of EOR techniques, reservoirs containing heavier crude oils tend to be more amenable to thermal EOR methods, which heat the crude oil to reduce its viscosity and thus decrease the mobility ratio. The increased heat reduces the surface tension of the oil and increases the permeability of the oil. A summary of various EOR techniques is presented in Table 1.
TABLE 1. Enhanced Oil Recovery (EOR) Techniques CSS Cyclic Steam Stimulation or "huff and puff." Steam is injected into a well at a temperature of 300-340 C for a period of weeks to months. The well is allowed to sit for days to weeks to allow heat to soak into the formation, and, later, the hot oil is pumped out of the well for weeks or months. Once the production rate falls off, the well is put through another cycle of steam injection, soak and production. This process is repeated until the cost of injecting steam becomes higher than the money made from producing oil. Recovery factors are around 20 to 25%, but the cost to inject steam is high.
SAGD Steam Assisted Gravity Drainage uses at least two horizontal wells--one at the bottom of the formation and another about 5 meters above it. Steam is injected into the upper well, the heat melts the heavy oil, which allows it to drain by gravity into the lower well, where it is pumped to the surface. SAGD is cheaper than CSS, allows very high oil production rates, and recovers up to 60% of the oil in place.
VAPEX Vapor Extraction Process is similar to SAGD, but instead of steam, hydrocarbon solvents are injected into an upper well to dilute heavy oil and enables the diluted heavy oil to flow into a lower well.
ISO In situ combustion involves a burning of a small amount of the oil in situ, the heat thereby mobilizing the heavy oil.
THAI Toe to Heel Air Injection is an ISO method that combines a vertical air injection well with a horizontal production well. The process ignites oil in the reservoir and creates a vertical wall of fire moving from the "toe" of the horizontal well toward the "heel", which burns the heavier oil components and upgrades some of the heavy bitumen into lighter oil right in the formation.
COGD Combustion Overhead Gravity Drainage is another ISO method that employs a number of vertical air injection wells above a horizontal production well located at the base of the bitumen pay zone. An initial Steam Cycle similar to CSS is used to prepare the bitumen for ignition and mobility. Following that cycle, air is injected into the vertical wells, igniting the upper bitumen and mobilizing (through heating) the lower bitumen to flow into the production well. It is expected that COGD will result in water savings of 80% compared to SAGD.
EM A variety of electromagnetic methods of heating oil in situ are also being developed.
GAS A variety of gas injection methods are also used or being developed, including INJECTION the use of cryogenic gases.
COMBO Any of the above methods can be used in combination.
FIELD OF THE INVENTION
[0003] The invention relates to methods of improving the effectiveness of wet in situ combustion (ISC) processes to accelerate oil production and particularly to an improved wet in situ combustion process utilizing foam. Water containing a foaming agent is injected along with an oxygen-containing gas to maintain a consistent water-gas ratio, to facilitate water-reservoir rock contact and to prevent separation of water and gas.
BACKGROUND OF THE INVENTION
[0004] Conventional oil reserves are preferred sources of oil because they provide a high ratio of extracted energy over energy used in regards to the extraction and refining processes it undergoes. Unfortunately, due to the physics of fluid flow, not all conventional oil can be produced. Additionally, as conventional oil sources become scarce or economically non-viable due to depletion, unconventional oil sources are becoming a potential supply of oil. But, unconventional oil production is also problematic because it consists of extra heavy oils having a consistency ranging from that of heavy molasses to a solid at room temperature and may also be located in the reservoir rocks. These properties make it difficult to simply pump the oil out of the ground; thus, its production is a less efficient process than conventional oil.
[0005] As a result, enhanced oil recovery (EOR) techniques are often employed to increase the amount of subterranean crude oil extracted. Using EOR, 30-60% or more of the original oil can be extracted. Additionally, EOR finds applications in both conventional and unconventional oil reserves.
[0006] During EOR, compounds not naturally found in the reservoir are injected into the reservoir in a well other than the producing well to assist in oil recovery.
Simply stated, EOR
techniques overcome the physical forces holding the oil hydrocarbons underground. There are many types of EOR techniques that are categorized by the compound being injection: gas injection, chemical injection, microbial injection or thermal recovery. While there are many types of EOR techniques, reservoirs containing heavier crude oils tend to be more amenable to thermal EOR methods, which heat the crude oil to reduce its viscosity and thus decrease the mobility ratio. The increased heat reduces the surface tension of the oil and increases the permeability of the oil. A summary of various EOR techniques is presented in Table 1.
TABLE 1. Enhanced Oil Recovery (EOR) Techniques CSS Cyclic Steam Stimulation or "huff and puff." Steam is injected into a well at a temperature of 300-340 C for a period of weeks to months. The well is allowed to sit for days to weeks to allow heat to soak into the formation, and, later, the hot oil is pumped out of the well for weeks or months. Once the production rate falls off, the well is put through another cycle of steam injection, soak and production. This process is repeated until the cost of injecting steam becomes higher than the money made from producing oil. Recovery factors are around 20 to 25%, but the cost to inject steam is high.
SAGD Steam Assisted Gravity Drainage uses at least two horizontal wells--one at the bottom of the formation and another about 5 meters above it. Steam is injected into the upper well, the heat melts the heavy oil, which allows it to drain by gravity into the lower well, where it is pumped to the surface. SAGD is cheaper than CSS, allows very high oil production rates, and recovers up to 60% of the oil in place.
VAPEX Vapor Extraction Process is similar to SAGD, but instead of steam, hydrocarbon solvents are injected into an upper well to dilute heavy oil and enables the diluted heavy oil to flow into a lower well.
ISO In situ combustion involves a burning of a small amount of the oil in situ, the heat thereby mobilizing the heavy oil.
THAI Toe to Heel Air Injection is an ISO method that combines a vertical air injection well with a horizontal production well. The process ignites oil in the reservoir and creates a vertical wall of fire moving from the "toe" of the horizontal well toward the "heel", which burns the heavier oil components and upgrades some of the heavy bitumen into lighter oil right in the formation.
COGD Combustion Overhead Gravity Drainage is another ISO method that employs a number of vertical air injection wells above a horizontal production well located at the base of the bitumen pay zone. An initial Steam Cycle similar to CSS is used to prepare the bitumen for ignition and mobility. Following that cycle, air is injected into the vertical wells, igniting the upper bitumen and mobilizing (through heating) the lower bitumen to flow into the production well. It is expected that COGD will result in water savings of 80% compared to SAGD.
EM A variety of electromagnetic methods of heating oil in situ are also being developed.
GAS A variety of gas injection methods are also used or being developed, including INJECTION the use of cryogenic gases.
COMBO Any of the above methods can be used in combination.
2 [0007] One technique less commonly used is in situ combustion (ISC), which involves the oxidative generation of heat within the reservoir itself. During a dry in situ combustion (FIG. 1), an oxygen-containing gas such as air is injected into an underground oil reservoir and burned with part of the hydrocarbons to create heat. The fire can be started by either lowering an incendiary device, such as a phosphorus bomb or a gas burner, into the well, or the injection of a large amount of air can cause spontaneous combustion. Once burning, large volumes of air, or other oxygen source gas, must be continually injected into the reservoir to sustain the fire. This combustion reaction also creates steam that, along with light hydrocarbons, condenses and releases heat to the nearby oil. During ISC, a frontal advance containing different layers of combustion gases, steam, and heated oil is created. This frontal advance acts as a production drive, thus driving the heated oil towards producing wells.
[0008] Fireflood projects are not extensively used due to the difficulty in controlling the flame front and a propensity to set the producing wells on fire. However, the method uses less freshwater, produces 50% less greenhouse gases, and has a smaller footprint than other production techniques. Thus, there is a certain interest in further developing combustion based methods for future use.
[0009] ISC can either be forward or reverse combustion. In forward combustion, the fire and injected oxygen source gas originate at the injection well. Thus, the gas flow, combustion front and oil flow advance in the same horizontal direction towards the producing well. In reverse combustion, the gas flow is counter-current to the combustion front.
[0010] The main cost associated with dry ISC is the cost of compression for the air injection system. Furthermore, the effectiveness of this technique depends on the velocity and stability of the frontal advance, as well as the heat generated from the combustion. During the dry ISC
process, as the oil is produced, depleted volumes remaining in the reservoir rock are primarily filled with air, steam and other gases resulting from the combustion. The rock absorbs much of the energy resulting from the heat of combustion reaction and heat of condensation of the steam.
Thus, this energy is wasted because it is not used to further produce oil, resulting in inefficiencies in the dry ISC process.
[0011] Other novel techniques have been developed to increase the efficiency of EOR oil production through the use of liquids instead of gases.
[0008] Fireflood projects are not extensively used due to the difficulty in controlling the flame front and a propensity to set the producing wells on fire. However, the method uses less freshwater, produces 50% less greenhouse gases, and has a smaller footprint than other production techniques. Thus, there is a certain interest in further developing combustion based methods for future use.
[0009] ISC can either be forward or reverse combustion. In forward combustion, the fire and injected oxygen source gas originate at the injection well. Thus, the gas flow, combustion front and oil flow advance in the same horizontal direction towards the producing well. In reverse combustion, the gas flow is counter-current to the combustion front.
[0010] The main cost associated with dry ISC is the cost of compression for the air injection system. Furthermore, the effectiveness of this technique depends on the velocity and stability of the frontal advance, as well as the heat generated from the combustion. During the dry ISC
process, as the oil is produced, depleted volumes remaining in the reservoir rock are primarily filled with air, steam and other gases resulting from the combustion. The rock absorbs much of the energy resulting from the heat of combustion reaction and heat of condensation of the steam.
Thus, this energy is wasted because it is not used to further produce oil, resulting in inefficiencies in the dry ISC process.
[0011] Other novel techniques have been developed to increase the efficiency of EOR oil production through the use of liquids instead of gases.
3 [0012] Water has also been utilized in dry ISC methods. A polymer colloidal system mixed with water was used to transport ozone gas into the reservoir. [1] This system allowed for quicker autoignition of the dry ISC process.
[0013] Also, the injection of water for a wet in situ combustion process (Fig. 2) has been found to improve oil production. In the wet ISC process, water and an oxygen gas source are injected together into the reservoir. The heat in the reservoir converts the water into steam. The generated steam from the water combines with the frontal advance to help drive the oil.
Additionally, water aids in scavenging the heat left in the reservoir rock after the combustion front has advanced through. The water is heated by the rock, which creates more steam that can condense in the burning front and transfer heat to nearby oil, resulting in increased oil production. The addition of injected water also reduces the gas injection rates, thereby reducing compression costs seen in dry ISC.
[0014] However, a disadvantage of the wet combustion process is the difficulty in maintaining proper water-gas ratios. If water-gas ratio is too low, then there is not enough water to effectively recover all of the available energy in the reservoir rock. If the water-gas ratio is too high, then there is too much water that is not converted into steam and interferes with the combustion front by cooling the temperature or extinguishing the combustion front. Thus, an optimum water-gas ratio would effectively recover the energy stored in the reservoir rock by converting the water to steam, but not cool or quench the combustion front such that it is extinguished. Furthermore, the proper ratio will all reduce the amount of fuel needed, which decreases the gas requirements needed to heat the oil.
[0015] Another disadvantage of the wet combustion process is the separation of water and the gas in the reservoir. This separation is also dependent on the water-gas ratio. If the water does not travel horizontally or vertically through the reservoir to scavenge the heat, then only gas will reach the combustion front, which will essentially be a dry combustion.
If there is too much water, then the gas cannot travel through the reservoir to reach the combustion front, thus potentially allowing water to extinguish the combustion front. Also, because water is denser, it could cumulate at the base of the reservoir and not reach hotter rock. As such, it is imperative that a proper water-gas ratio is maintained for the water and the as to travel together through the oil reserve for optimal oil production efficiencies.
[0013] Also, the injection of water for a wet in situ combustion process (Fig. 2) has been found to improve oil production. In the wet ISC process, water and an oxygen gas source are injected together into the reservoir. The heat in the reservoir converts the water into steam. The generated steam from the water combines with the frontal advance to help drive the oil.
Additionally, water aids in scavenging the heat left in the reservoir rock after the combustion front has advanced through. The water is heated by the rock, which creates more steam that can condense in the burning front and transfer heat to nearby oil, resulting in increased oil production. The addition of injected water also reduces the gas injection rates, thereby reducing compression costs seen in dry ISC.
[0014] However, a disadvantage of the wet combustion process is the difficulty in maintaining proper water-gas ratios. If water-gas ratio is too low, then there is not enough water to effectively recover all of the available energy in the reservoir rock. If the water-gas ratio is too high, then there is too much water that is not converted into steam and interferes with the combustion front by cooling the temperature or extinguishing the combustion front. Thus, an optimum water-gas ratio would effectively recover the energy stored in the reservoir rock by converting the water to steam, but not cool or quench the combustion front such that it is extinguished. Furthermore, the proper ratio will all reduce the amount of fuel needed, which decreases the gas requirements needed to heat the oil.
[0015] Another disadvantage of the wet combustion process is the separation of water and the gas in the reservoir. This separation is also dependent on the water-gas ratio. If the water does not travel horizontally or vertically through the reservoir to scavenge the heat, then only gas will reach the combustion front, which will essentially be a dry combustion.
If there is too much water, then the gas cannot travel through the reservoir to reach the combustion front, thus potentially allowing water to extinguish the combustion front. Also, because water is denser, it could cumulate at the base of the reservoir and not reach hotter rock. As such, it is imperative that a proper water-gas ratio is maintained for the water and the as to travel together through the oil reserve for optimal oil production efficiencies.
4 [0016] Finding the optimum water-gas ratio is difficult because the reservoir heterogeneities and gravity override can affect the fluid movement. Usually, water and gas injection rates are varied until a reasonable water-gas ratio is found. The rates are then adjusted throughout the wet ISC to maintain this ratio. This method produces inconsistent results, nor is there a method to quickly determine the proper ratio or injection rates.
[0017] US4691773 discloses a wet in situ combustion method wherein a non-oxygen containing fluid, such as water, is introduced along with air cyclically to produce periodic high volume rates of injected fluid. However, both techniques can result in over-injecting water and extinguishing the combustion front can occur, leading to a loss of time and money to re-start the process.
[0018] US7882893 discloses the use of surfactant, salt brine and oxygen to create a foam during ISC. The foam decreases the mobility of the displacing fluid (brine) in the higher permeability zones and diverts more oxygen-containing gas into the lower permeability zones.
Thus, the foam prevents the water from segregating from the oxygen gas. As the displacing fluid evaporates from the foam, the foam breaks and becomes an oxygen-rich steam and alkaline brine.
[0019] US20090194278 discloses an ISC technique that uses a surfactant-based foam that is injected with or prior to the oxygen gas. The purpose of the foam is to increase the amount of oxygen available for combustion and to control the mobility of the oxygen through the already swept zones. The foam also prevents the heated gas from seeping into porous sections of the reservoir. Furthermore, water or steam can be mixed with the foam to enhance the effectiveness of the oxygen utilization and displacement of oil. The focus of this technique is the prevention of heat transfer to the surrounding reservoir rock. It does not address the possibility of scavenging heat.
[0020] Therefore, what is needed in the art is a better method for maintaining water-gas ratios during the wet in situ combustion process and scavenging heat from rocks after the combustion front advances that also prevents separation of water and air.
SUMMARY OF THE DISCLOSURE
[0021] The present disclosure describes an improved wet ISC technique to recover oil from depleted reservoirs. During wet ISC, water containing a foaming agent, an oxygen-containing gas, and, optionally, additional gases, are injected into a subterranean oil containing reservoir.
The foaming agent aids in maintaining a consistent water-gas ratio and prevents separation of water and gas as they move through the reservoir.
BRIEF DESCRIPTION OF THE DRAWINGS
[0022] FIG. 1 is a schematic depicting dry forward in situ combustion.
[0023] FIG. 2 is a schematic depicting wet forward in situ combustion [0024] FIG. 3 is a schematic depicting foam-assisted wet forward in situ combustion DESCRIPTION OF EMBODIMENTS OF THE INVENTION
[0025] The disclosure relates to a heat scavenging method using an agent for forming foams/aerosols/hydrosols/other emulsions or colloidal dispersions. For conciseness hereafter hereafter, foaming agent is used for exemplary purposes only given possibility of creating the aerosols/hydrosols/other emulsions or colloidal dispersions.
[0026] Generally, the invention provides an improved wet in situ combustion process in which a foaming agent is injected together with the water. The novel feature of this improved method is the ability of the foam to carry water through the reservoir and combustion zone. The foaming agent has a low density and viscosity, which can efficiently carry water into overburden rock. The use of such a foaming agent ensures proper water-to-oxygen-containing gas ratios are maintained during wet in situ combustion by carrying water throughout the reservoir. Consistent water-to-oxygen ratios will allow for maximum heat scavenging and minimum combustion quenching by the water. Another advantage of using foam to carry water through the reservoir is an increase in contact between the water and heated reservoir rock. This will create more steam, which will heat the oil and allow for greater production of oil. The foam will also prevent the water from pooling.
[0027] Additionally, the foam will also prevent the water and gas from separating in the reservoir, thus preventing a dry ISC process. Additionally, the foam can also contain oxygen, which will help in providing a consistent amount of oxygen to the combustion front.
[0028] In a preferred embodiment, the oxygen-containing gas is air. Further preferred embodiments include generating foam on the surface before injection into the subterranean oil formation.
[0029] In one embodiment, the water being mixed with the foaming agent is brine water recovered from the reservoir being treated. Alternatively, surface water or sea water can be used.
[0030] In another embodiment, the foaming agent contains oxygen, which will aid in maintaining a consistent amount of oxygen at the combustion front.
[0031] In yet another embodiment, the water and foaming agent are injected some time after the oxygen-containing gas and optional additional gases have been injected into the subterranean formation.
[0032] In the present disclosure, the foaming agent can generate foam on the surface before injection into the oil formation. In another variation, the foaming agent can generate foam in situ in the subsurface after injection into the oil formation.
[0033] The invention also describes the use of the above methods to recover more oil from steam assisted gravity drainage (SAGD) depleted reservoirs.
[0034] The foaming agent can include, but is not limited to, other colloidal foams, aerosols, hydrosols, emulsions, or dispersions capable of creating a suitable foam.
Preferred foam components have thermal and chemical properties that are stable at the high temperatures (>200 C) used in ISC and should have low adsorption onto reservoir rock/clay surfaces.
Additionally, the foaming capabilities should be effective at the particular reservoir brine pH.
Thus, the foaming agent can be any foaming agent that is stable under reservoir conditions, and increases the transport of water, thus maintaining a consistent water-to-gas ratio.
[0035] Foam agents can be surfactant- or alkali-based. Thermally and chemically stable, non-ionic, anionic, cationic, and amphoteric/zwitterionic surfactants including, but are not limited to, alkyl benzene, aromatic sulfonates, alpha/internal olefin, sulfonates, alkyl aryl sulfonates, and alkoxy sulfates can be used. High alkyl chain lengths should be chosen since the efficiency of foam generation increases with increases in chain length.
[0036] Examples of alkali-based components are alkaline metal carbonates, bicarbonates and hydroxides, including but not limited to, sodium carbonate, sodium bicarbonate, sodium hydroxide, potassium carbonate, potassium bicarbonate, potassium hydroxide, magnesium carbonate, and calcium carbonate.
[0037] Other agents that can be used are in other colloidal foams, aerosols, hydrosols, emulsions, or dispersions which could create a suitable and stable foam.
[0038] The chosen foaming agent will depend of the characteristics of the reservoir. Because the foaming agent is being used to increase the sweep efficiency of the water/gases, the foaming agent should not react with the formation. For example, cationic and amphoteric surfactants have strong interactions with sand particles, thus they would not be ideal foaming agents for a sandy reservoir. Interactions with reservoir formation will result in an increase in concentration of foaming agent and will be cost prohibited, or at least less cost effective.
[0039] The chosen foaming agent also depends on the water. High salinity water can cause precipitation of surfactant molecules, especially when high divalent ion concentrations are present. Non-ionic surfactants and alkali-based surfactants are considered to be more resistant to high salinity water.
[0040] Many high temperature surfactant- and alkali-based foaming agents are commercially available from vendors such as BASF, ChemEOR Inc., Down Chemical Company, Huntsman Corporation, OilChem Technologies, Sasol and Tiorco.
[0041] The desired properties of the generated foam arc densities in the range of 0.000598 ¨
0.0770 g/cm3 and viscosities in the range of 0.0123 ¨ 0.0216 cP. The lightness of the foam enables it to transport/lift the water and gas(es) being injected instead of blocking the high permeability zones in the reservoir. This will maintain the water-gas ratio as it moves through the reservoir.
[0042] The foam can be generated on the surface or sub-surface. Sub-surface methods for generating foam include a static mixer downhole, foam generation through a perforation in the well, natural mixing in the well, in situ foam generation in the reservoir or any combination thereof.
[0043] Additionally, the foaming agent/water mix can be injected at the same time as the gas(es), or can be injected some time after the gas(es) has been injected.
Furthermore, the foaming agent/water can be injected continuously or in slugs. Also, the foaming agent/water can be injected into vertical or horizontal wells to improve the wet ISC process, including both forward and reverse combustion.
[0044] An oxygen-containing gas is injected to fuel the combustion process in the reservoir.
Typical gases include air, oxygen, carbon dioxide, carbon monoxide or any combination thereof.
An additional non-oxygen containing gas can also be injected to fill in gas drive, including hydrogen, nitrogen, methane, hydrogen sulfide, propane, butane, natural gas, flue gas and any combination thereof. Gases may be in a liquid form, a liquid/gas mixture, or gas form.
[0045] As used herein, "oil," "crude oil," and "hydrocarbons" are used interchangeable to describe the hydrocarbons remaining in oil reservoirs after conventional drilling methods.
[0046] As used herein, "foaming agent" means an additive to water used to generate foam either above the surface before injection or sub-surface using a mechanical or natural mixing method. The additive can include, but is not limited to, colloidal foams, aerosols, hydrosols, emulsions, or dispersions.
[0047] As used herein, "oxygen-containing gas" or "oxygen source gas" mean a gas containing oxygen and capable of igniting and fueling the combustion front within the reservoir.
[0048] The use of the word "a" or "an" when used in conjunction with the term "comprising"
in the claims or the specification means one or more than one, unless the context dictates otherwise.
[0049] The term "about" means the stated value plus or minus the margin of error of measurement or plus or minus 10% if no method of measurement is indicated.
[0050] The use of the term "or" in the claims is used to mean "and/or"
unless explicitly indicated to refer to alternatives only or if the alternatives are mutually exclusive.
[0051] The terms "comprise", "have", "include" and "contain" (and their variants) are open-ended linking verbs and allow the addition of other elements when used in a claim.
[0052] The phrase "consisting of" is closed, and excludes all additional elements.
[0053] The phrase "consisting essentially of' excludes additional material elements, but allows the inclusions of non-material elements that do not substantially change the nature of the invention.
[0054] The following abbreviations are used herein:
ABBREVIATION TERM
ISC In situ combustion SAGD Steam assisted gravity drainage PSI Pounds per square inch [0055] Fig. 1 depicts a dry forward ISC. Here, dry air is injected into a reservoir to fuel the combustion process and help push the combustion front towards the oil production well. Note that the heat formed during the combustion process is absorbed by the reservoir rock. Also, the heated oil bank, i.e. displaced oil, has not traveled close to the oil production well.
[0056] In contrast, the addition of water to the air injection results in the contact of water with heated reservoir rock, as shown in Fig. 2. After contacting the heated rock, the water is converted into steam and is pushed forward the water-air injection. As the steam contacts cooler rock in the reservoir, it condenses and transfers heat to the nearby oil. This additional heat results in the heated oil bank travelling further towards the oil production well then the dry forward ISC
depicted in Fig. 1.
[0057] Fig. 3 depicts the present invention¨use of a foaming agent in the water. Here, the foaming agent helps carry the water into the reservoir, thus facilitating increased contact with the heated reservoir rock. Furthermore, the foam also prevents the water and air from separating due to differences in density. As before, the resulting steam heats the oil;
however, the increased water/rock contact has allowed water to scavenge more heat from the rock to transfer to the oil.
As such, the oil is able to move towards the oil production well more efficiently than either a water-air injection or air only injection.
[0058] Reference is made to the following:
[0059] 1. Limkar, Parikshit S., "Novel In-Situ Combustion Technique Using a Semi-Permeable Igniter Assembly," Society of Petroleum Engineers, SPE 125583, 2009.
[0060] 2. Burger, Jacques G., Sahuquet, Bernard C., "Laboratory Research on Wet Combustion," Journal of Petroleum Technology, 1973, 1137-46.
[0061] 3. Falls, Andrew H., Lawson, Jimmie B. and Hirasaki, George J., "The Role of Noncondensable Gas in Steam Foams", Journal of Petroleum Technology, January 1988.
[0062] US3993133 [0063] US3994345 [0064] US4691773 [0065] US7882893 [0066] US20090194278
[0017] US4691773 discloses a wet in situ combustion method wherein a non-oxygen containing fluid, such as water, is introduced along with air cyclically to produce periodic high volume rates of injected fluid. However, both techniques can result in over-injecting water and extinguishing the combustion front can occur, leading to a loss of time and money to re-start the process.
[0018] US7882893 discloses the use of surfactant, salt brine and oxygen to create a foam during ISC. The foam decreases the mobility of the displacing fluid (brine) in the higher permeability zones and diverts more oxygen-containing gas into the lower permeability zones.
Thus, the foam prevents the water from segregating from the oxygen gas. As the displacing fluid evaporates from the foam, the foam breaks and becomes an oxygen-rich steam and alkaline brine.
[0019] US20090194278 discloses an ISC technique that uses a surfactant-based foam that is injected with or prior to the oxygen gas. The purpose of the foam is to increase the amount of oxygen available for combustion and to control the mobility of the oxygen through the already swept zones. The foam also prevents the heated gas from seeping into porous sections of the reservoir. Furthermore, water or steam can be mixed with the foam to enhance the effectiveness of the oxygen utilization and displacement of oil. The focus of this technique is the prevention of heat transfer to the surrounding reservoir rock. It does not address the possibility of scavenging heat.
[0020] Therefore, what is needed in the art is a better method for maintaining water-gas ratios during the wet in situ combustion process and scavenging heat from rocks after the combustion front advances that also prevents separation of water and air.
SUMMARY OF THE DISCLOSURE
[0021] The present disclosure describes an improved wet ISC technique to recover oil from depleted reservoirs. During wet ISC, water containing a foaming agent, an oxygen-containing gas, and, optionally, additional gases, are injected into a subterranean oil containing reservoir.
The foaming agent aids in maintaining a consistent water-gas ratio and prevents separation of water and gas as they move through the reservoir.
BRIEF DESCRIPTION OF THE DRAWINGS
[0022] FIG. 1 is a schematic depicting dry forward in situ combustion.
[0023] FIG. 2 is a schematic depicting wet forward in situ combustion [0024] FIG. 3 is a schematic depicting foam-assisted wet forward in situ combustion DESCRIPTION OF EMBODIMENTS OF THE INVENTION
[0025] The disclosure relates to a heat scavenging method using an agent for forming foams/aerosols/hydrosols/other emulsions or colloidal dispersions. For conciseness hereafter hereafter, foaming agent is used for exemplary purposes only given possibility of creating the aerosols/hydrosols/other emulsions or colloidal dispersions.
[0026] Generally, the invention provides an improved wet in situ combustion process in which a foaming agent is injected together with the water. The novel feature of this improved method is the ability of the foam to carry water through the reservoir and combustion zone. The foaming agent has a low density and viscosity, which can efficiently carry water into overburden rock. The use of such a foaming agent ensures proper water-to-oxygen-containing gas ratios are maintained during wet in situ combustion by carrying water throughout the reservoir. Consistent water-to-oxygen ratios will allow for maximum heat scavenging and minimum combustion quenching by the water. Another advantage of using foam to carry water through the reservoir is an increase in contact between the water and heated reservoir rock. This will create more steam, which will heat the oil and allow for greater production of oil. The foam will also prevent the water from pooling.
[0027] Additionally, the foam will also prevent the water and gas from separating in the reservoir, thus preventing a dry ISC process. Additionally, the foam can also contain oxygen, which will help in providing a consistent amount of oxygen to the combustion front.
[0028] In a preferred embodiment, the oxygen-containing gas is air. Further preferred embodiments include generating foam on the surface before injection into the subterranean oil formation.
[0029] In one embodiment, the water being mixed with the foaming agent is brine water recovered from the reservoir being treated. Alternatively, surface water or sea water can be used.
[0030] In another embodiment, the foaming agent contains oxygen, which will aid in maintaining a consistent amount of oxygen at the combustion front.
[0031] In yet another embodiment, the water and foaming agent are injected some time after the oxygen-containing gas and optional additional gases have been injected into the subterranean formation.
[0032] In the present disclosure, the foaming agent can generate foam on the surface before injection into the oil formation. In another variation, the foaming agent can generate foam in situ in the subsurface after injection into the oil formation.
[0033] The invention also describes the use of the above methods to recover more oil from steam assisted gravity drainage (SAGD) depleted reservoirs.
[0034] The foaming agent can include, but is not limited to, other colloidal foams, aerosols, hydrosols, emulsions, or dispersions capable of creating a suitable foam.
Preferred foam components have thermal and chemical properties that are stable at the high temperatures (>200 C) used in ISC and should have low adsorption onto reservoir rock/clay surfaces.
Additionally, the foaming capabilities should be effective at the particular reservoir brine pH.
Thus, the foaming agent can be any foaming agent that is stable under reservoir conditions, and increases the transport of water, thus maintaining a consistent water-to-gas ratio.
[0035] Foam agents can be surfactant- or alkali-based. Thermally and chemically stable, non-ionic, anionic, cationic, and amphoteric/zwitterionic surfactants including, but are not limited to, alkyl benzene, aromatic sulfonates, alpha/internal olefin, sulfonates, alkyl aryl sulfonates, and alkoxy sulfates can be used. High alkyl chain lengths should be chosen since the efficiency of foam generation increases with increases in chain length.
[0036] Examples of alkali-based components are alkaline metal carbonates, bicarbonates and hydroxides, including but not limited to, sodium carbonate, sodium bicarbonate, sodium hydroxide, potassium carbonate, potassium bicarbonate, potassium hydroxide, magnesium carbonate, and calcium carbonate.
[0037] Other agents that can be used are in other colloidal foams, aerosols, hydrosols, emulsions, or dispersions which could create a suitable and stable foam.
[0038] The chosen foaming agent will depend of the characteristics of the reservoir. Because the foaming agent is being used to increase the sweep efficiency of the water/gases, the foaming agent should not react with the formation. For example, cationic and amphoteric surfactants have strong interactions with sand particles, thus they would not be ideal foaming agents for a sandy reservoir. Interactions with reservoir formation will result in an increase in concentration of foaming agent and will be cost prohibited, or at least less cost effective.
[0039] The chosen foaming agent also depends on the water. High salinity water can cause precipitation of surfactant molecules, especially when high divalent ion concentrations are present. Non-ionic surfactants and alkali-based surfactants are considered to be more resistant to high salinity water.
[0040] Many high temperature surfactant- and alkali-based foaming agents are commercially available from vendors such as BASF, ChemEOR Inc., Down Chemical Company, Huntsman Corporation, OilChem Technologies, Sasol and Tiorco.
[0041] The desired properties of the generated foam arc densities in the range of 0.000598 ¨
0.0770 g/cm3 and viscosities in the range of 0.0123 ¨ 0.0216 cP. The lightness of the foam enables it to transport/lift the water and gas(es) being injected instead of blocking the high permeability zones in the reservoir. This will maintain the water-gas ratio as it moves through the reservoir.
[0042] The foam can be generated on the surface or sub-surface. Sub-surface methods for generating foam include a static mixer downhole, foam generation through a perforation in the well, natural mixing in the well, in situ foam generation in the reservoir or any combination thereof.
[0043] Additionally, the foaming agent/water mix can be injected at the same time as the gas(es), or can be injected some time after the gas(es) has been injected.
Furthermore, the foaming agent/water can be injected continuously or in slugs. Also, the foaming agent/water can be injected into vertical or horizontal wells to improve the wet ISC process, including both forward and reverse combustion.
[0044] An oxygen-containing gas is injected to fuel the combustion process in the reservoir.
Typical gases include air, oxygen, carbon dioxide, carbon monoxide or any combination thereof.
An additional non-oxygen containing gas can also be injected to fill in gas drive, including hydrogen, nitrogen, methane, hydrogen sulfide, propane, butane, natural gas, flue gas and any combination thereof. Gases may be in a liquid form, a liquid/gas mixture, or gas form.
[0045] As used herein, "oil," "crude oil," and "hydrocarbons" are used interchangeable to describe the hydrocarbons remaining in oil reservoirs after conventional drilling methods.
[0046] As used herein, "foaming agent" means an additive to water used to generate foam either above the surface before injection or sub-surface using a mechanical or natural mixing method. The additive can include, but is not limited to, colloidal foams, aerosols, hydrosols, emulsions, or dispersions.
[0047] As used herein, "oxygen-containing gas" or "oxygen source gas" mean a gas containing oxygen and capable of igniting and fueling the combustion front within the reservoir.
[0048] The use of the word "a" or "an" when used in conjunction with the term "comprising"
in the claims or the specification means one or more than one, unless the context dictates otherwise.
[0049] The term "about" means the stated value plus or minus the margin of error of measurement or plus or minus 10% if no method of measurement is indicated.
[0050] The use of the term "or" in the claims is used to mean "and/or"
unless explicitly indicated to refer to alternatives only or if the alternatives are mutually exclusive.
[0051] The terms "comprise", "have", "include" and "contain" (and their variants) are open-ended linking verbs and allow the addition of other elements when used in a claim.
[0052] The phrase "consisting of" is closed, and excludes all additional elements.
[0053] The phrase "consisting essentially of' excludes additional material elements, but allows the inclusions of non-material elements that do not substantially change the nature of the invention.
[0054] The following abbreviations are used herein:
ABBREVIATION TERM
ISC In situ combustion SAGD Steam assisted gravity drainage PSI Pounds per square inch [0055] Fig. 1 depicts a dry forward ISC. Here, dry air is injected into a reservoir to fuel the combustion process and help push the combustion front towards the oil production well. Note that the heat formed during the combustion process is absorbed by the reservoir rock. Also, the heated oil bank, i.e. displaced oil, has not traveled close to the oil production well.
[0056] In contrast, the addition of water to the air injection results in the contact of water with heated reservoir rock, as shown in Fig. 2. After contacting the heated rock, the water is converted into steam and is pushed forward the water-air injection. As the steam contacts cooler rock in the reservoir, it condenses and transfers heat to the nearby oil. This additional heat results in the heated oil bank travelling further towards the oil production well then the dry forward ISC
depicted in Fig. 1.
[0057] Fig. 3 depicts the present invention¨use of a foaming agent in the water. Here, the foaming agent helps carry the water into the reservoir, thus facilitating increased contact with the heated reservoir rock. Furthermore, the foam also prevents the water and air from separating due to differences in density. As before, the resulting steam heats the oil;
however, the increased water/rock contact has allowed water to scavenge more heat from the rock to transfer to the oil.
As such, the oil is able to move towards the oil production well more efficiently than either a water-air injection or air only injection.
[0058] Reference is made to the following:
[0059] 1. Limkar, Parikshit S., "Novel In-Situ Combustion Technique Using a Semi-Permeable Igniter Assembly," Society of Petroleum Engineers, SPE 125583, 2009.
[0060] 2. Burger, Jacques G., Sahuquet, Bernard C., "Laboratory Research on Wet Combustion," Journal of Petroleum Technology, 1973, 1137-46.
[0061] 3. Falls, Andrew H., Lawson, Jimmie B. and Hirasaki, George J., "The Role of Noncondensable Gas in Steam Foams", Journal of Petroleum Technology, January 1988.
[0062] US3993133 [0063] US3994345 [0064] US4691773 [0065] US7882893 [0066] US20090194278
Claims (14)
1. An in situ combustion method of recovery of hydrocarbons from a subterranean oil containing formation penetrated by at least one injection well and at least one production well, which comprises:
igniting the hydrocarbons to form a combustion front by injecting oxygen-containing gas and heat into the formation through an injection well;
injecting a water and oxygen-containing gas through an injection well and in contact with a fluid that is at least one of a foam, an aerosol, a hydrosol, an emulsion and a colloidal dispersion and has a density and viscosity to carry the water via buoyancy forces to maintain a wet in situ combustion process wherein the density of the fluid is between 0.000598 - 0.0770 g/cm3 and the viscosity of the fluid is between 0.0123 - 0.0216 cP; and recovering hydrocarbons and other fluids at a production well.
igniting the hydrocarbons to form a combustion front by injecting oxygen-containing gas and heat into the formation through an injection well;
injecting a water and oxygen-containing gas through an injection well and in contact with a fluid that is at least one of a foam, an aerosol, a hydrosol, an emulsion and a colloidal dispersion and has a density and viscosity to carry the water via buoyancy forces to maintain a wet in situ combustion process wherein the density of the fluid is between 0.000598 - 0.0770 g/cm3 and the viscosity of the fluid is between 0.0123 - 0.0216 cP; and recovering hydrocarbons and other fluids at a production well.
2. The method of claim 1, further comprising injecting an agent into the injection well to form the fluid in situ.
3. The method of claim 2, wherein said agent is a surfactant.
4. The method of claim 3, wherein the surfactant is chosen from a group consisting of alkyl benzene, aromatic sulfonates, alpha/internal olefin, sulfonates, alkyl aryl sulfonates, alkoxy sulfates and any combination thereof.
5. The method of claim 2, wherein said agent is an alkali-based salt.
6. The method of claim 5, wherein the alkali-based salt is chosen from a group consisting of sodium carbonate, sodium bicarbonate, sodium hydroxide, potassium carbonate, potassium bicarbonate, potassium hydroxide, magnesium carbonate, calcium carbonate and any combination thereof.
7. The method of claim 2, wherein said water containing said agent is injected continuously.
8. The method of claim 2, wherein said water containing the agent is injected into vertical or horizontal wells.
9. The method of claim 2, wherein said water containing said agent is injected in a slug.
10. The method of claim 1, wherein said water comprises oilfield brine, produced water, seawater, aquifer water, or riverwater.
11. The method of claim 1, further comprising injecting a non-oxygen-containing gas.
12. The method of claim 1, further comprising injecting hydrogen, nitrogen, methane, hydrogen sulfide, propane, butane, natural gas, flue gas, or any combination thereof, and wherein said oxygen-containing gas is air, oxygen, carbon dioxide, carbon monoxide, or any combination thereof.
13. An in situ combustion method of recovery of hydrocarbons from a Steam Assisted Gravity Drainage (SAGD) depleted reservoir penetrated by at least one injection well and at least one production well, which comprises:
igniting the hydrocarbons to form a combustion front by injecting oxygen-containing gas and heat into the formation through an injection well;
scavenging heat from a rock formation by injecting a water containing an agent to generate a fluid that is at least one of a foam, an aerosol, a hydrosol, an emulsion and a colloidal dispersion to maintain a wet in situ combustion process wherein a density of the fluid is between 0.000598 - 0.0770 g/cm3 and a viscosity of the fluid is between 0.0123 -0.0216 cP; and, recovering hydrocarbons and other fluids at a production well.
igniting the hydrocarbons to form a combustion front by injecting oxygen-containing gas and heat into the formation through an injection well;
scavenging heat from a rock formation by injecting a water containing an agent to generate a fluid that is at least one of a foam, an aerosol, a hydrosol, an emulsion and a colloidal dispersion to maintain a wet in situ combustion process wherein a density of the fluid is between 0.000598 - 0.0770 g/cm3 and a viscosity of the fluid is between 0.0123 -0.0216 cP; and, recovering hydrocarbons and other fluids at a production well.
14. An improved method of wet in situ combustion oil recovery, the method comprising igniting oil in a formation to form a burning front and injecting water behind said burning front to capture heat and drive oil towards a production well, wherein the improvement comprises injecting water behind said burning front and in contact with a fluid that is at least one of a foam, an aerosol, a hydrosol, an emulsion and a colloidal dispersion and has a density and viscosity to carry the water via buoyancy forces to maintain a wet in situ combustion process wherein the density of the fluid is between 0.000598 - 0.0770 g/cm3 and the viscosity is between 0.0123 -0.0216 cP.
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BR112014009436A2 (en) | 2011-10-21 | 2017-04-11 | Nexen Energy Ulc | oxygen-assisted gravity assisted steam drainage processes |
CA2815737C (en) | 2012-05-15 | 2020-05-05 | Nexen Inc. | Steam assisted gravity drainage with added oxygen geometry for impaired bitumen reservoirs |
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CN110144202B (en) * | 2019-06-14 | 2021-11-23 | 长江大学 | High-temperature high-pressure profile control and flooding long-acting foam and preparation method thereof |
CN113137218B (en) * | 2020-01-16 | 2023-05-26 | 中国石油天然气股份有限公司 | Method and device for determining position of fire flooding front edge of fire flooding gas injection well |
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US3565175A (en) * | 1969-10-16 | 1971-02-23 | Union Oil Co | Method for reducing gravity segregation of an aqueous flooding fluid |
US5129457A (en) * | 1991-03-11 | 1992-07-14 | Marathon Oil Company | Enhanced liquid hydrocarbon recovery process |
US7882893B2 (en) * | 2008-01-11 | 2011-02-08 | Legacy Energy | Combined miscible drive for heavy oil production |
CA2653099A1 (en) * | 2008-02-06 | 2009-08-06 | L'air Liquide-Societe Anonyme Pour L'etude Et L'exploitation Des Procede S Georges Claude | Enhanced oil recovery in oxygen based in situ combustion using foaming agents |
WO2010042719A2 (en) * | 2008-10-08 | 2010-04-15 | Potter Drilling, Inc. | Methods and apparatus for mechanical and thermal drilling |
WO2014110168A1 (en) * | 2013-01-08 | 2014-07-17 | Conocophillips Company | Heat scavenging method for thermal recovery processes |
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2014
- 2014-01-08 CA CA2897402A patent/CA2897402C/en active Active
- 2014-01-08 WO PCT/US2014/010718 patent/WO2014110157A1/en active Application Filing
- 2014-01-08 US US14/150,359 patent/US20140190689A1/en not_active Abandoned
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US20140190689A1 (en) | 2014-07-10 |
WO2014110157A1 (en) | 2014-07-17 |
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