US3175609A - Secondary recovery process with gas-liquid drive agents - Google Patents
Secondary recovery process with gas-liquid drive agents Download PDFInfo
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- US3175609A US3175609A US117813A US11781361A US3175609A US 3175609 A US3175609 A US 3175609A US 117813 A US117813 A US 117813A US 11781361 A US11781361 A US 11781361A US 3175609 A US3175609 A US 3175609A
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- 238000011084 recovery Methods 0.000 title claims description 20
- 239000007788 liquid Substances 0.000 title claims description 8
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 40
- 239000003208 petroleum Substances 0.000 claims description 32
- 239000002904 solvent Substances 0.000 claims description 32
- 238000000034 method Methods 0.000 claims description 27
- 239000011148 porous material Substances 0.000 claims description 27
- 238000002347 injection Methods 0.000 claims description 17
- 239000007924 injection Substances 0.000 claims description 17
- XLYOFNOQVPJJNP-PWCQTSIFSA-N Tritiated water Chemical compound [3H]O[3H] XLYOFNOQVPJJNP-PWCQTSIFSA-N 0.000 claims 1
- 239000007789 gas Substances 0.000 description 30
- 235000019441 ethanol Nutrition 0.000 description 11
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 6
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 6
- 239000012530 fluid Substances 0.000 description 6
- 239000000470 constituent Substances 0.000 description 5
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 4
- 150000001298 alcohols Chemical class 0.000 description 4
- 229930195733 hydrocarbon Natural products 0.000 description 4
- 150000002430 hydrocarbons Chemical class 0.000 description 4
- 239000000203 mixture Substances 0.000 description 4
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 3
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- 150000001299 aldehydes Chemical class 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 150000002576 ketones Chemical class 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- HCFAJYNVAYBARA-UHFFFAOYSA-N 4-heptanone Chemical compound CCCC(=O)CCC HCFAJYNVAYBARA-UHFFFAOYSA-N 0.000 description 2
- ZTQSAGDEMFDKMZ-UHFFFAOYSA-N Butyraldehyde Chemical compound CCCC=O ZTQSAGDEMFDKMZ-UHFFFAOYSA-N 0.000 description 2
- FERIUCNNQQJTOY-UHFFFAOYSA-N Butyric acid Chemical compound CCCC(O)=O FERIUCNNQQJTOY-UHFFFAOYSA-N 0.000 description 2
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 2
- DKGAVHZHDRPRBM-UHFFFAOYSA-N Tert-Butanol Chemical compound CC(C)(C)O DKGAVHZHDRPRBM-UHFFFAOYSA-N 0.000 description 2
- -1 alcohols Chemical class 0.000 description 2
- BTANRVKWQNVYAZ-UHFFFAOYSA-N butan-2-ol Chemical compound CCC(C)O BTANRVKWQNVYAZ-UHFFFAOYSA-N 0.000 description 2
- 238000010790 dilution Methods 0.000 description 2
- 239000012895 dilution Substances 0.000 description 2
- XBDQKXXYIPTUBI-UHFFFAOYSA-N dimethylselenoniopropionate Natural products CCC(O)=O XBDQKXXYIPTUBI-UHFFFAOYSA-N 0.000 description 2
- 239000008398 formation water Substances 0.000 description 2
- KQNPFQTWMSNSAP-UHFFFAOYSA-N isobutyric acid Chemical compound CC(C)C(O)=O KQNPFQTWMSNSAP-UHFFFAOYSA-N 0.000 description 2
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 2
- 229910052757 nitrogen Inorganic materials 0.000 description 2
- 150000007524 organic acids Chemical class 0.000 description 2
- 235000005985 organic acids Nutrition 0.000 description 2
- FDPIMTJIUBPUKL-UHFFFAOYSA-N pentan-3-one Chemical compound CCC(=O)CC FDPIMTJIUBPUKL-UHFFFAOYSA-N 0.000 description 2
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 2
- 239000004215 Carbon black (E152) Substances 0.000 description 1
- UGFAIRIUMAVXCW-UHFFFAOYSA-N Carbon monoxide Chemical compound [O+]#[C-] UGFAIRIUMAVXCW-UHFFFAOYSA-N 0.000 description 1
- OTMSDBZUPAUEDD-UHFFFAOYSA-N Ethane Chemical compound CC OTMSDBZUPAUEDD-UHFFFAOYSA-N 0.000 description 1
- 241000237858 Gastropoda Species 0.000 description 1
- 235000003332 Ilex aquifolium Nutrition 0.000 description 1
- 241000209027 Ilex aquifolium Species 0.000 description 1
- AMQJEAYHLZJPGS-UHFFFAOYSA-N N-Pentanol Chemical class CCCCCO AMQJEAYHLZJPGS-UHFFFAOYSA-N 0.000 description 1
- 241000184339 Nemophila maculata Species 0.000 description 1
- NBBJYMSMWIIQGU-UHFFFAOYSA-N Propionic aldehyde Chemical compound CCC=O NBBJYMSMWIIQGU-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 239000003570 air Substances 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 230000002542 deteriorative effect Effects 0.000 description 1
- 238000006073 displacement reaction Methods 0.000 description 1
- 125000005909 ethyl alcohol group Chemical group 0.000 description 1
- 230000002349 favourable effect Effects 0.000 description 1
- 239000003546 flue gas Substances 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 239000003345 natural gas Substances 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 238000005192 partition Methods 0.000 description 1
- 238000004391 petroleum recovery Methods 0.000 description 1
- 235000019260 propionic acid Nutrition 0.000 description 1
- IUVKMZGDUIUOCP-BTNSXGMBSA-N quinbolone Chemical compound O([C@H]1CC[C@H]2[C@H]3[C@@H]([C@]4(C=CC(=O)C=C4CC3)C)CC[C@@]21C)C1=CCCC1 IUVKMZGDUIUOCP-BTNSXGMBSA-N 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- HGBOYTHUEUWSSQ-UHFFFAOYSA-N valeric aldehyde Natural products CCCCC=O HGBOYTHUEUWSSQ-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K8/00—Compositions for drilling of boreholes or wells; Compositions for treating boreholes or wells, e.g. for completion or for remedial operations
- C09K8/58—Compositions for enhanced recovery methods for obtaining hydrocarbons, i.e. for improving the mobility of the oil, e.g. displacing fluids
Definitions
- this invention teaches a process for the recovery of oil from reservoirs containing high concentrations of reservoir water comprising the steps of first injecting a slug of a gas which is substantially insoluble in the petroleum contained in the reservoir, then injecting a quantity of a solvent which is soluble in both petroleum and floodwater, and finally injecting floodwater to drive the gas and solvent through the formation to a producing well.
- the purpose of the gas injection prior to the solvent injection is to reduce the water saturation in a large portion of the area which will be contacted by the solvent.
- the reservoir to be treated contains water in the amount of about 0.5 pore volume or more, the disrupting effects of the gas injected prior to the miscible solvent is minimized, and the efiiciency of the process is enhanced by the reduction in water saturation, the avoidance or" loss of solvent into the reservoir water, and by the avoidance of dilution of solvent at the leading edge of the solventflood front, which would otherwise render the iiood ineffective.
- a slug of gas having low solubility in petroleum in the amount of about 0.1 to 0.5 reservoir pore volume, is first injected through an input well into a petroleum reservoir having an initial reservoir water content of about 0.5 pore volume or greater.
- the volume of gas injected must be sufficient to substantially displace the formation water and maintain effective buffer between the formation water and the later-injected solvent. in general, the lowest effective amount of gas will be most suitable, since the injection of a gas slug larger than is required could have an adverse effect upon the sweep efliciency of the process, thereby preventing maximum oil recovery. While quantities of gas in the range of 0.1 to 0.5 pore volume may be employed, in most instances it is preferred to use not more than about 0.2 pore volume of gas, measured at injection temperature and pressure.
- the volume of solvent injected is not critical, but quantities less than 0.03 pore volume are seldom effective, and quantities in excess of about 0.2 pore volume add to the expense of the process without producing a proportionate increase in the oil ultimately recovered.
- floodwater is injected in a conventional manner to drive the previously injected gas and solvent slugs towards the producing well. This final Water injection is continued until the water-to-oil ratio at the producing well rises to such a level that further oil recovery becomes uneconomical, at which time injection is terminated.
- This process is applicable to any of the standard flooding patterns, such as the line-drive, five-spot, or nine-spot systems. While not essential, it is preferred that the producing wells be closed in during the period of gas injection, to minimize fingering of the gas through the reservoir and reduce the unfavorable effects of the high mobility of the gas upon sweep efficiency, and further to enhance the effectiveness of the gas in preventin dilution of solvent by reservoir water.
- gases are available which may be used in carrying out the process of this invention.
- the gas chosen must have a solubility in petroleum not greater than about 2% by weight at reservoir temperature and pressure, and should be substantially inert, that, is chemically non-reactive under reservoir conditions. It is also desirable, but not essential, that the gas have a solubility not greater than about 10% by weight in water.
- gases include, but are not limited to, nitrogen, flue gas, air, and natural gas which is substantially free of components heavier than ethane.
- the solvent a Wide variety of materials are available which may be used as the solvent, it being required only that the solvent be liquid in physical state, be capable of dissolving at least about 10% its weight of petroleum, and be soluble in water to the extent of at least 10% of the Weight of the water.
- the solvent will be miscible with both petroleum oil and Water, and still more preferably will have in addition a partition coefficient favoring solution in oil when in the presence of both oil and water.
- suitable solvents are partially oxidized hydrocarbons such as alcohols, including tert-butanol, sec-butanol, n-butanol,
- isopropanol, n-propanol, and pentanols Other suitable materials include ketones, such as methyl ethyl ketone, diethyl ketone, and di-n-propyl ketone; aldehydes such as aoetaldehyde, propanal, and butyraldehyde; and organic acids, such as acetic acid, propionic acid, butyric acid, and isobutyric acid. Mixtures of the aforenamed liquids may also be used in the process of this invention.
- ketones such as methyl ethyl ketone, diethyl ketone, and di-n-propyl ketone
- aldehydes such as aoetaldehyde, propanal, and butyraldehyde
- organic acids such as acetic acid, propionic acid, butyric acid, and isobutyric acid. Mixtures of the aforenamed liquids may also
- Mixtures of partially oxidized hydrocarbons produced by hydrocarbon oxidation processes comprising a wide variety of alcohols, aldehydes, ketones, acids, and other constituents, may be used provided the weighted average of the solubilities of the constituents in petroleum is suitably high.
- Such mixtures may contain minor amounts of materials having a low solubility in petroleum, such as methyl and ethyl alcohols, provided the quantities of such constituents are not excessive, and other more soluble constituents are present in quantity.
- Mixtures of C to C alcohols, ketones, aldehydes, and organic acids are suitable.
- the core was reconstituted to have an oil saturation of about 0.62 pore volume, and a water saturation of about 0.38 pore volume.
- the cores of these examples were waterflooded to the water and oil saturations stated in these examples. Except as set out in the examples, the test conditions were substantially identical in each case.
- Example I A Berea sandstone core having a water saturation of 0.62 pore volume and an oil saturation of 0.38 pore volume was flooded by first injecting 0.25 pore volume of isopropanol, and then driving the isopropanol through the core by the injection of water.
- the water-toil ratio in the fluids produced from the core reached a value of 100-to-1
- the oil recovery was found to be 31.6% of the oil initially in place, indicating poor efliciency was achieved when the initial water saturation of the core was high.
- the residual oil remaining after this flood was about 26% pore volume.
- Example II A Berea sandstone core having a water saturation of 0.39 pore volume and an oil saturation of 0.62 pore volume was flooded in a manner substantially identical to that used in Example I. When the water-to-oil ratio reached a value of 100-to-1, the oil recovery was found to be 45.9% of the oil in place, indicating higher flooding efiiciency was achieved when the initial Water saturation of the core was low.
- Example III to-oil ratio then again increased, and when it reached a value of about 100-to-1, the total quantity of oil recovery during operation was found to be 45% of the oil initially in place. This recovery was much higher than that obtained using the same amount of alcohol in treating a high-water-content core (Example 1), without the air-injection step. The oil recovery also was as favorable as that obtained when treating a core having a low initial water saturation (Example II) using the same quantity of the same solvent. In each example, the flood was terminated when the water-to-oil ratio in the produced fluids reached a value of l00-to-1. Since the recovery of oil at such excessive water-to-oil ratios is not commercially attractive, the relative efiiciency of the processes beyond this point is immaterial.
- a method for the recovery of petroleum oil from reservoirs containing water in excess of about 0.5 pore volume and petroleum comprising injecting through an input well into said reservoir about 0.1 to 0.2 pore volume or" a gas having a solubility in petroleum not greater than about 2% by weight, immediately thereafter injecting about 0.03 to 0.20 pore volume of a liquid solvent capable of dissolving at least about 10% its weight of petroleum and soluble in water to at least the extent of 10% of the Weight of the water, driving said solvent through the reservoir by the injection of floodwater, and producing petroleum from an output well.
- liquid solvent consists essentially of oxygenated hydrocarbons having 3 to 7 carbon atoms per molecule.
- a method of recovery of petroleum oil from reservoirs containing water in excess of about 0.5 pore volume and petroleum comprising injecting through an input well and into said reservoir about 0.1 to 0.2 pore volume of a gas having a low solubility in petroleum, immediately, thereafter injecting about 0.03 to 0.20 pore volume of a liquid solvent having a high solubility in water and in petroleum, driving said solvent through the reservoir by the injection of floodwater, and producing petroleum from an output well.
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- Chemical & Material Sciences (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Organic Chemistry (AREA)
- Production Of Liquid Hydrocarbon Mixture For Refining Petroleum (AREA)
Description
United States Patent This invention relates to the recovery of petroleum from reservoirs beneath the surface of the earth, and is more particularly concerned with a flooding process for recovering petroleum in reater amounts than is possible by conventio al flooding methods.
It is well known in the secondary recovery art to inject a slug of fluid which is rriscible with both the petroleum oil and the water phases in the reservoir, and to drive the slug of fluid through the reservoir by injecting floodwater behind it. Typical of the fluids used in such secondary recovery processes are the lower alcohols. When the fluid is an alcohol, for example, and it is attempted to form and maintain zones of oil-mcohol and wateralcohol miscibility, with a buffer zone of alcohol main tained between the aforementioned zones as they move through the reservoir from the injection well to the produeing well, serious ditiiculties are encountered.
The presence of large volumes of water in the reservoir hinders the removal of the petroleum by such misciblephase flooding processes because alcohol dissolves into the reservoir water, deteriorating the alcohol slug. Because of the high solubility of the injected solvent in reservoir Water, the leading edge of the solvent zone becomes diluted with water, and the solvent Zone may break down entirely, with the result that the oil-tosolvent-to-water miscible-phase displacement is lost. This results in lower oil recovery, or causes high water-to-oil production ratios at the producing well, and increases the alcohol requirement for a given petroleum recovery.
Briefly, this invention teaches a process for the recovery of oil from reservoirs containing high concentrations of reservoir water comprising the steps of first injecting a slug of a gas which is substantially insoluble in the petroleum contained in the reservoir, then injecting a quantity of a solvent which is soluble in both petroleum and floodwater, and finally injecting floodwater to drive the gas and solvent through the formation to a producing well. The purpose of the gas injection prior to the solvent injection is to reduce the water saturation in a large portion of the area which will be contacted by the solvent.
It is an object of this invention to provide an improved method for the secondary recovery of oil from underground reservoirs. Another object of this invention is to provide a method for recovering a higher percentage of the petroleum in re ervoirs which contain high concentrations of water.
The inject on of gas having a low solubility in petroleum oil prior to the injection of a liquid solvent which is soluble in both the petroleum oil and the subsequently injected floodwater is contrary to principles taught in the prior art. The prior art considers that the injection of a highly mobile gas before the injection of a miscible solvent results in disruption of continuity in the oil phase in the reservoir, tends to result in reater fingering and bypassing of oil-containing zones, and thereby reduces flood eificiency. It has nevertheless been found that where the reservoir to be treated contains water in the amount of about 0.5 pore volume or more, the disrupting effects of the gas injected prior to the miscible solvent is minimized, and the efiiciency of the process is enhanced by the reduction in water saturation, the avoidance or" loss of solvent into the reservoir water, and by the avoidance of dilution of solvent at the leading edge of the solventflood front, which would otherwise render the iiood ineffective. Accordingly, ias been found that by injecting a gas slug of suitable size prior to the injection of the miscible solvent, when treating reservoirs having a water concentration of not less than about 0.5 pore volume, the efficiency of recovery is raised to a value approximating that obtainable when misciblephase recovery using the same solvent, in the same amount, is carried out in a. reservoir of low water content.
In carrying out the process of this invention, a slug of gas having low solubility in petroleum, in the amount of about 0.1 to 0.5 reservoir pore volume, is first injected through an input well into a petroleum reservoir having an initial reservoir water content of about 0.5 pore volume or greater. The volume of gas injected must be sufficient to substantially displace the formation water and maintain effective buffer between the formation water and the later-injected solvent. in general, the lowest effective amount of gas will be most suitable, since the injection of a gas slug larger than is required could have an adverse effect upon the sweep efliciency of the process, thereby preventing maximum oil recovery. While quantities of gas in the range of 0.1 to 0.5 pore volume may be employed, in most instances it is preferred to use not more than about 0.2 pore volume of gas, measured at injection temperature and pressure.
A slug of a suitable solvent which is soluble in both petroleum oil and Water, and preferably is miscible with both oil and water, is injected into the reservoir behind the first-injected gas. The volume of solvent injected is not critical, but quantities less than 0.03 pore volume are seldom effective, and quantities in excess of about 0.2 pore volume add to the expense of the process without producing a proportionate increase in the oil ultimately recovered. Finally, floodwater is injected in a conventional manner to drive the previously injected gas and solvent slugs towards the producing well. This final Water injection is continued until the water-to-oil ratio at the producing well rises to such a level that further oil recovery becomes uneconomical, at which time injection is terminated. This process is applicable to any of the standard flooding patterns, such as the line-drive, five-spot, or nine-spot systems. While not essential, it is preferred that the producing wells be closed in during the period of gas injection, to minimize fingering of the gas through the reservoir and reduce the unfavorable effects of the high mobility of the gas upon sweep efficiency, and further to enhance the effectiveness of the gas in preventin dilution of solvent by reservoir water.
A wide variety of gases are available which may be used in carrying out the process of this invention. The gas chosen must have a solubility in petroleum not greater than about 2% by weight at reservoir temperature and pressure, and should be substantially inert, that, is chemically non-reactive under reservoir conditions. It is also desirable, but not essential, that the gas have a solubility not greater than about 10% by weight in water. Suitable gases include, but are not limited to, nitrogen, flue gas, air, and natural gas which is substantially free of components heavier than ethane. Similarly, a Wide variety of materials are available which may be used as the solvent, it being required only that the solvent be liquid in physical state, be capable of dissolving at least about 10% its weight of petroleum, and be soluble in water to the extent of at least 10% of the Weight of the water. Preferably the solvent will be miscible with both petroleum oil and Water, and still more preferably will have in addition a partition coefficient favoring solution in oil when in the presence of both oil and water. Typical suitable solvents are partially oxidized hydrocarbons such as alcohols, including tert-butanol, sec-butanol, n-butanol,
isopropanol, n-propanol, and pentanols. Other suitable materials include ketones, such as methyl ethyl ketone, diethyl ketone, and di-n-propyl ketone; aldehydes such as aoetaldehyde, propanal, and butyraldehyde; and organic acids, such as acetic acid, propionic acid, butyric acid, and isobutyric acid. Mixtures of the aforenamed liquids may also be used in the process of this invention. Mixtures of partially oxidized hydrocarbons produced by hydrocarbon oxidation processes, comprising a wide variety of alcohols, aldehydes, ketones, acids, and other constituents, may be used provided the weighted average of the solubilities of the constituents in petroleum is suitably high. Such mixtures may contain minor amounts of materials having a low solubility in petroleum, such as methyl and ethyl alcohols, provided the quantities of such constituents are not excessive, and other more soluble constituents are present in quantity. Mixtures of C to C alcohols, ketones, aldehydes, and organic acids are suitable.
The effectiveness of the method of this invention has been established by three comparative examples. In each case the core was reconstituted to have an oil saturation of about 0.62 pore volume, and a water saturation of about 0.38 pore volume. In order to obtain high water saturation cores for use in Examples I and III, the cores of these examples were waterflooded to the water and oil saturations stated in these examples. Except as set out in the examples, the test conditions were substantially identical in each case.
Example I A Berea sandstone core having a water saturation of 0.62 pore volume and an oil saturation of 0.38 pore volume was flooded by first injecting 0.25 pore volume of isopropanol, and then driving the isopropanol through the core by the injection of water. When the water-toil ratio in the fluids produced from the core reached a value of 100-to-1, the oil recovery was found to be 31.6% of the oil initially in place, indicating poor efliciency was achieved when the initial water saturation of the core was high. The residual oil remaining after this flood was about 26% pore volume.
Example II A Berea sandstone core having a water saturation of 0.39 pore volume and an oil saturation of 0.62 pore volume was flooded in a manner substantially identical to that used in Example I. When the water-to-oil ratio reached a value of 100-to-1, the oil recovery was found to be 45.9% of the oil in place, indicating higher flooding efiiciency was achieved when the initial Water saturation of the core was low.
Example III to-oil ratio then again increased, and when it reached a value of about 100-to-1, the total quantity of oil recovery during operation was found to be 45% of the oil initially in place. This recovery was much higher than that obtained using the same amount of alcohol in treating a high-water-content core (Example 1), without the air-injection step. The oil recovery also was as favorable as that obtained when treating a core having a low initial water saturation (Example II) using the same quantity of the same solvent. In each example, the flood was terminated when the water-to-oil ratio in the produced fluids reached a value of l00-to-1. Since the recovery of oil at such excessive water-to-oil ratios is not commercially attractive, the relative efiiciency of the processes beyond this point is immaterial.
The embodiments of the invention in which an exclu sive property or privilege is claimed are defined as follows:
1. A method for the recovery of petroleum oil from reservoirs containing water in excess of about 0.5 pore volume and petroleum comprising injecting through an input well into said reservoir about 0.1 to 0.2 pore volume or" a gas having a solubility in petroleum not greater than about 2% by weight, immediately thereafter injecting about 0.03 to 0.20 pore volume of a liquid solvent capable of dissolving at least about 10% its weight of petroleum and soluble in water to at least the extent of 10% of the Weight of the water, driving said solvent through the reservoir by the injection of floodwater, and producing petroleum from an output well.
2. The method in accordance with claim 1 in which the principal constituent of said gas is nitrogen.
3. The method in accordance with claim 2 in which said gas is air.
4. The method in accordance with claim 3 in which said producing well is shut in while air is injected through the input well.
5. The method in accordance with claim 1 in which said liquid solvent consists essentially of oxygenated hydrocarbons having 3 to 7 carbon atoms per molecule.
6. The method in accordance with claim 5 in which said gas is air and the amount of air injected is about 0.1 to 0.2 pore volume.
7. The method in accordance with claim 6 in which the volume of solvent injected is about 0.1 pore volume.
8. A method of recovery of petroleum oil from reservoirs containing water in excess of about 0.5 pore volume and petroleum comprising injecting through an input well and into said reservoir about 0.1 to 0.2 pore volume of a gas having a low solubility in petroleum, immediately, thereafter injecting about 0.03 to 0.20 pore volume of a liquid solvent having a high solubility in water and in petroleum, driving said solvent through the reservoir by the injection of floodwater, and producing petroleum from an output well.
9. A method in accordance with claim 8 in which said producing well is shut in while gas is injected through the input well.
10. A method in accordance with claim 9 in which said gas is air.
References Cited by the Examiner UNITED STATES PATENTS 2,973,811 3/61 Rogers 1669 X 3,033,288 5/62 Holm 1669 3,03 6,631 5/62 Holbrook 166-9 CHARLES E. OCONNELL, Primary Examiner.
Claims (1)
1. A METHOD FOR THE RECOVERY OF PETROLEUM OIL FROM RESERVOIRS CONTAINING WATER IN EXCESS OF ABOUT 0.5 PORE VOLUME AND PETROLEUM COMPRISING INJECTING THROUGH AN INPUT WELL INTO SAID RESERVOIR ABOUT 0.1 TO 0.2 PORE VOLUME OF A GAS HAVING A SOLUBILITY IN PETROLEUM NOT GREATER THAN ABOUT 2% BY WEIGHT, IMMEDIATELY THEREAFTER INJECTING ABOUT 0.03 TO 0.20 PORE VOLUME OF A LIQUID SOLVENT CAPABLE OF DISSOLVING AT LEAST ABOUT 10% ITS WEIGHT OF PETROLEUM AND SOLUBLE IN WATER TO AT LEAST THE EXTENT OF 10% OF THE WEIGHT OF THE WATER, DRIVING SAID SOLVENT THROUGH THE RESERVOIR BY THE INJECTION OF FLOODWATER, AND PRODUCING PETROLEUM FROM AN OUTPUT WELL.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US117813A US3175609A (en) | 1961-06-19 | 1961-06-19 | Secondary recovery process with gas-liquid drive agents |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US117813A US3175609A (en) | 1961-06-19 | 1961-06-19 | Secondary recovery process with gas-liquid drive agents |
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| Publication Number | Publication Date |
|---|---|
| US3175609A true US3175609A (en) | 1965-03-30 |
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| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US117813A Expired - Lifetime US3175609A (en) | 1961-06-19 | 1961-06-19 | Secondary recovery process with gas-liquid drive agents |
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Cited By (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3311167A (en) * | 1963-11-21 | 1967-03-28 | Union Oil Co | Secondary recovery technique |
| US3330342A (en) * | 1964-03-16 | 1967-07-11 | Union Oil Co | Secondary recovery process for low pressure oil-bearing reservoirs |
| US3482632A (en) * | 1968-03-15 | 1969-12-09 | Union Oil Co | Miscible flooding process using improved soluble oil compositions |
| US3500918A (en) * | 1968-03-15 | 1970-03-17 | Union Oil Co | Miscible flooding process using improved soluble oil compositions |
| US3525395A (en) * | 1968-12-26 | 1970-08-25 | Mobil Oil Corp | Alternate gas and water flood process for recovering oil |
Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2973811A (en) * | 1957-11-25 | 1961-03-07 | Phillips Petroleum Co | Process for detecting underground water |
| US3033288A (en) * | 1958-12-29 | 1962-05-08 | Pure Oil Co | Secondary recovery of oil from underground reservoirs |
| US3036631A (en) * | 1959-02-19 | 1962-05-29 | Pure Oil Co | Water-flooding process |
-
1961
- 1961-06-19 US US117813A patent/US3175609A/en not_active Expired - Lifetime
Patent Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2973811A (en) * | 1957-11-25 | 1961-03-07 | Phillips Petroleum Co | Process for detecting underground water |
| US3033288A (en) * | 1958-12-29 | 1962-05-08 | Pure Oil Co | Secondary recovery of oil from underground reservoirs |
| US3036631A (en) * | 1959-02-19 | 1962-05-29 | Pure Oil Co | Water-flooding process |
Cited By (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3311167A (en) * | 1963-11-21 | 1967-03-28 | Union Oil Co | Secondary recovery technique |
| US3330342A (en) * | 1964-03-16 | 1967-07-11 | Union Oil Co | Secondary recovery process for low pressure oil-bearing reservoirs |
| US3482632A (en) * | 1968-03-15 | 1969-12-09 | Union Oil Co | Miscible flooding process using improved soluble oil compositions |
| US3500918A (en) * | 1968-03-15 | 1970-03-17 | Union Oil Co | Miscible flooding process using improved soluble oil compositions |
| US3525395A (en) * | 1968-12-26 | 1970-08-25 | Mobil Oil Corp | Alternate gas and water flood process for recovering oil |
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