AU4058402A - Improved enhanced oil recovery - Google Patents
Improved enhanced oil recovery Download PDFInfo
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- AU4058402A AU4058402A AU40584/02A AU4058402A AU4058402A AU 4058402 A AU4058402 A AU 4058402A AU 40584/02 A AU40584/02 A AU 40584/02A AU 4058402 A AU4058402 A AU 4058402A AU 4058402 A AU4058402 A AU 4058402A
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- oil
- carbon dioxide
- gas mixture
- volume
- nitrogen
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- 238000011084 recovery Methods 0.000 title claims description 32
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 claims description 214
- 229910002092 carbon dioxide Inorganic materials 0.000 claims description 111
- 239000007789 gas Substances 0.000 claims description 102
- 239000001569 carbon dioxide Substances 0.000 claims description 90
- 239000000203 mixture Substances 0.000 claims description 77
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 70
- 238000000034 method Methods 0.000 claims description 67
- 229910052757 nitrogen Inorganic materials 0.000 claims description 34
- 238000002347 injection Methods 0.000 claims description 33
- 239000007924 injection Substances 0.000 claims description 33
- 230000015572 biosynthetic process Effects 0.000 claims description 30
- 238000004519 manufacturing process Methods 0.000 claims description 24
- 239000011261 inert gas Substances 0.000 claims description 17
- 239000003570 air Substances 0.000 claims description 16
- 229930195733 hydrocarbon Natural products 0.000 claims description 15
- 150000002430 hydrocarbons Chemical class 0.000 claims description 15
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 10
- 229910001868 water Inorganic materials 0.000 claims description 10
- 230000002708 enhancing effect Effects 0.000 claims description 9
- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 claims description 8
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 8
- 239000001301 oxygen Substances 0.000 claims description 8
- 229910052760 oxygen Inorganic materials 0.000 claims description 8
- 239000012530 fluid Substances 0.000 claims description 7
- 229910052786 argon Inorganic materials 0.000 claims description 4
- 239000001307 helium Substances 0.000 claims description 4
- 229910052734 helium Inorganic materials 0.000 claims description 4
- SWQJXJOGLNCZEY-UHFFFAOYSA-N helium atom Chemical compound [He] SWQJXJOGLNCZEY-UHFFFAOYSA-N 0.000 claims description 4
- 239000000463 material Substances 0.000 claims description 4
- MYMOFIZGZYHOMD-UHFFFAOYSA-N Dioxygen Chemical compound O=O MYMOFIZGZYHOMD-UHFFFAOYSA-N 0.000 claims description 2
- 238000002485 combustion reaction Methods 0.000 claims description 2
- 238000000926 separation method Methods 0.000 claims description 2
- 239000003643 water by type Substances 0.000 claims description 2
- 239000012267 brine Substances 0.000 claims 2
- HPALAKNZSZLMCH-UHFFFAOYSA-M sodium;chloride;hydrate Chemical compound O.[Na+].[Cl-] HPALAKNZSZLMCH-UHFFFAOYSA-M 0.000 claims 2
- -1 steam Substances 0.000 claims 2
- 238000011065 in-situ storage Methods 0.000 claims 1
- 239000003921 oil Substances 0.000 description 111
- 238000005755 formation reaction Methods 0.000 description 18
- 239000005662 Paraffin oil Substances 0.000 description 12
- 230000000694 effects Effects 0.000 description 10
- 239000004215 Carbon black (E152) Substances 0.000 description 8
- UFWIBTONFRDIAS-UHFFFAOYSA-N Naphthalene Chemical compound C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 description 8
- 239000010692 aromatic oil Substances 0.000 description 6
- 230000001965 increasing effect Effects 0.000 description 5
- 239000011148 porous material Substances 0.000 description 5
- 230000008569 process Effects 0.000 description 5
- 230000008961 swelling Effects 0.000 description 5
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 4
- 239000012188 paraffin wax Substances 0.000 description 4
- 239000011435 rock Substances 0.000 description 4
- RWSOTUBLDIXVET-UHFFFAOYSA-N Dihydrogen sulfide Chemical compound S RWSOTUBLDIXVET-UHFFFAOYSA-N 0.000 description 2
- ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 description 2
- 125000003118 aryl group Chemical group 0.000 description 2
- 230000008901 benefit Effects 0.000 description 2
- 229910001873 dinitrogen Inorganic materials 0.000 description 2
- 239000003546 flue gas Substances 0.000 description 2
- 229910000037 hydrogen sulfide Inorganic materials 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 230000004048 modification Effects 0.000 description 2
- 238000012986 modification Methods 0.000 description 2
- 230000007704 transition Effects 0.000 description 2
- 241000254032 Acrididae Species 0.000 description 1
- OTMSDBZUPAUEDD-UHFFFAOYSA-N Ethane Chemical compound CC OTMSDBZUPAUEDD-UHFFFAOYSA-N 0.000 description 1
- 238000010793 Steam injection (oil industry) Methods 0.000 description 1
- KPAMAAOTLJSEAR-UHFFFAOYSA-N [N].O=C=O Chemical compound [N].O=C=O KPAMAAOTLJSEAR-UHFFFAOYSA-N 0.000 description 1
- 239000008346 aqueous phase Substances 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- GUJOJGAPFQRJSV-UHFFFAOYSA-N dialuminum;dioxosilane;oxygen(2-);hydrate Chemical compound O.[O-2].[O-2].[O-2].[Al+3].[Al+3].O=[Si]=O.O=[Si]=O.O=[Si]=O.O=[Si]=O GUJOJGAPFQRJSV-UHFFFAOYSA-N 0.000 description 1
- 239000008246 gaseous mixture Substances 0.000 description 1
- 230000003993 interaction Effects 0.000 description 1
- 239000007791 liquid phase Substances 0.000 description 1
- 239000001294 propane Substances 0.000 description 1
- 238000005086 pumping Methods 0.000 description 1
- 238000004088 simulation Methods 0.000 description 1
- 238000002791 soaking Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 125000005931 tert-butyloxycarbonyl group Chemical group [H]C([H])([H])C(OC(*)=O)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
Classifications
-
- E—FIXED CONSTRUCTIONS
- E21—EARTH OR ROCK DRILLING; MINING
- E21B—EARTH OR ROCK 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
- E21B43/164—Injecting CO2 or carbonated water
Landscapes
- Engineering & Computer Science (AREA)
- Mining & Mineral Resources (AREA)
- Geology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Fluid Mechanics (AREA)
- Environmental & Geological Engineering (AREA)
- Chemical & Material Sciences (AREA)
- Physics & Mathematics (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Life Sciences & Earth Sciences (AREA)
- Geochemistry & Mineralogy (AREA)
- Production Of Liquid Hydrocarbon Mixture For Refining Petroleum (AREA)
- Physical Or Chemical Processes And Apparatus (AREA)
- Treating Waste Gases (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Description
-1-
AUSTRALIA
PATENTS ACT 1990 COMPLETE SPECIFICATION FOR A STANDARD PATENT
ORIGINAL
Name of Applicant: Actual Inventor/s: Address for Service:
CCN:
The BOC Group, Inc Shuen-Cheng Hwang and Kirk Walton Limbach and Ramakrishnan Ramachandran BALDWIN SHELSTON WATERS MARGARET STREET SYDNEY NSW 2000 3710000352 IMPROVED ENHANCED OIL RECOVERY Invention Title: The following statement is a full description of this invention, including the best method of performing it known to us:- File: 35276AUP00 IMPROVED ENHANCED OIL RECOVERY FIELD OF THE INVENTION The present invention provides for a method for enhancing the recovery of oil from underground formations. More particularly, the present invention provides for injecting into the oil in the underground formation a gas mixture which contains at least 50% by volume carbon dioxide and the remainder nitrogen or other inert gas.
BACKGROUND OF THE INVENTION Oil or gas and any water which is contained in the porous rock surrounding the oil or gas in a reservoir or formation are typically under pressure due to the weight of the material above them. As such, they will move to an area of lower pressure and higher elevation such as the well head. After some pressure has been released, the oil may still flow to the surface but it does so more slowly. This movement can be helped along by a mechanical pump such as the grasshopper pumps one often sees. These processes are typically referred to as primary oil recovery. Typically, less than 50% of the oil in the oil formation is recovered by primary techniques.
Recovery can be increased by pursuing enhanced oil recovery (EOR) methods. Typically, these methods are divided into two groups: secondary and tertiary.
Secondary EOR generally refers to pumping a fluid, either liquid or gas, into the ground to build back pressure that was dissipated during primary recovery. The most common of these methods is to inject water and is simply called a waterflood.
The tertiary recovery schemes typically use chemical interactions or heat to either reduce the oil viscosity so the oil flows more freely or to change the properties of the interface between the oil and the surrounding rock pores so that the oil can flow out of the small pores in the rock and enter larger channels where the oil can be swept by a driving fluid or move by pressure gradient to a production well. The oil may also be swelled so that a portion of the oil emerges from small pores into the channels or larger pores in the rock.
Typical of these processes are steam injection, miscible fluid injection and surfactant injection.
Thermal techniques employing steam can be utilized in a well to well scheme or also in a single-well technique which is know as the huff and puff method. In this method, steam is injected via a well in a quantity sufficient to heat the subterranean hydrocarbon-bearing formation in the vicinity of the well. The well is then shut in for a soaking period after which it is placed on production. After production has declined, the huff and puff method may again be employed on the same well to again stimulate production.
The use of carbon dioxide and its injection into oil reservoirs is known for well to well and single well production enhancement. The carbon dioxide dissolves in the oil easily and causes the oil to swell and reduces the viscosity and surface tension of the oil which in turn leads to additional oil recovery.
The carbon dioxide may also be employed with steam such that the steam and carbon dioxide are injected either simultaneously or sequentially, often followed by a soak period, followed by a further injection of carbon dioxide or other fluids.
US 2,623,596 describes enhanced recovery using gases in an injection well with oil recovery from a separate production well. Enhanced recovery using CO2 and N2 mixtures is discussed with data presented showing oil recovery increasing monotonically as CO2% in the gas mixture is increased.
However, the data presented does not demonstrate results when between CO2 and 100% CO2, is employed.
US Patent 3,295,601 teaches that a slug of gas consisting of carbon dioxide and hydrocarbon gases, preferably of two to four carbon atoms, or nitrogen, air, hydrogen sulfide, flue gases and similar gases in a gas mixture, when injected in a well, establishes a transition zone. This transition zone is then driven through the injection well by a driving fluid which will produce oil from the stratum and reduce viscous fingering. The preferred slug of gas consists of 50% carbon dioxide and a substantial concentration of C2 to C4 hydrocarbon gases such as 10 to 50% by volume. It appears that the remainder of the gases in this gas mixture are selected from the group consisting of nitrogen, air, hydrogen sulfide and flue gases and similar gases would make up the balance in the preferred composition of carbon dioxide and C2 to C4 hydrocarbon gas.
US Patent 5,725,054 teaches a method for recovering oil from a subterranean formation by injecting into said well a gas mixture which comprises carbon dioxide and a gas selected from the group consisting of methane, nitrogen and mixtures thereof. The gas mixture comprises about to about 50% by volume of carbon dioxide. As noted in the examples, the highest percentages were 50% by volume carbon dioxide.
The present inventors have discovered that the use of carbon dioxide in percentages greater than 50%, up to 99%, along with nitrogen or another inert gas as the remainder of the gas mixture will enhance oil production.
SUMMARY OF THE INVENTION The present invention provides for a method for enhancing the recovery of oil from an underground formation comprising injecting into the oil a gas mixture comprising at least 50% by volume of carbon dioxide and an inert gas. The present invention further provides for a method for enhancing the recovery of oil from an underground formation comprising injecting into the oil a gas mixture comprising carbon dioxide and nitrogen wherein the carbon dioxide is present in the gas mixture in an amount of at least 50% by volume. In addition, the present invention will provide for a method for lowering the viscosity and surface tension as well as increasing the volume or swelling of the oil in an underground formation comprising injecting into the oil a gas mixture comprising at least 50% by volume carbon dioxide and an inert gas.
BRIEF DESCRIPTION OF THE DRAWINGS Fig. 1 is a graphical representation of the effect of carbon dioxide content of gas on paraffin oil viscosity.
Fig. 2 is a graphical representation of carbon dioxide content of gas on naphthene oil viscosity.
Fig. 3 is a graphical representation of carbon dioxide content of gas on aromatic oil viscosity.
Fig. 4 is a graphical representation of carbon dioxide content of gas on paraffin oil surface tension.
Fig. 5 is a graphical representation of carbon dioxide content of gas on naphthene oil surface tension.
Fig. 6 is a graphical representation of carbon dioxide content of gas on aromatic oil surface tension.
Fig. 7 is a graphical representation of carbon dioxide content of gas on paraffin oil viscosity at various temperatures.
Fig. 8 is a graphical representation of carbon dioxide content of gas on paraffin oil surface tension at various temperatures.
Fig. 9 is a graphical representation of carbon dioxide content of gas on paraffin oil volume at various temperatures.
DETAILED DESCRIPTION OF THE INVENTION The present invention comprises a method for enhancing the recovery of oil from an underground formation comprising injecting into the oil a gas mixture comprising at least 50% by volume carbon dioxide and an inert gas.
The inert gas is preferably nitrogen. Other inert gases such as helium and argon may also be employed. The present invention also comprises a method for enhancing the recovery of oil from an underground formation comprising injecting into the oil a gas mixture which comprises carbon dioxide and nitrogen. The carbon dioxide is present in the gas mixture in an amount of at least 50% by volume. The introduction of a combination of carbon dioxide and nitrogen gas to the formation provides an unexpected advantage of lower oil viscosity and surface tension than the introduction of carbon dioxide or nitrogen alone. This will also provide greater oil swelling than the use of carbon dioxide or nitrogen alone. The use of nitrogen adds an economic advantage to the mixture as there is lower cost than that for pure carbon dioxide consumption.
For purposes of the present invention, Applicants define oil as being a hydrocarbon which comprises paraffin, aromatic or naphthene constituents or mixtures thereof.
The mixture of the carbon dioxide and nitrogen will be injected into the formation containing the oil at a pressure of 100 pounds per square inch to 20,000 pounds per square inch depending upon the depth of the oil reservoir.
This injection method allows for use of WAG (water alternating gas) well-towell process whereby an injection of gas is followed by a waterflood to drive the oil and enhance production at the well head. This injection method will also work in a huff and puff process. In the huff and puff process, the mixture would be injected into the formation. The formation would then be sealed allowing a soak period of determinate length of time, followed by an improved oil recovery or production period.
The mixtures of carbon dioxide and nitrogen may be created by any means. Preferably, a carbon dioxide-rich stream and a nitrogen-rich stream are combined or a hydrocarbon is combusted using air or oxygen-enriched air to produce the carbon dioxide. The present inventors assert that in addition to nitrogen, other inert gases, when combined with carbon dioxide in an optimum ratio, will minimize oil viscosity and surface tension while increasing swelling.
One means for producing the carbon dioxide-rich gas stream involves the use of a power plant or co-generation plant at or near the well site.
Oxygen-enriched air and hydrocarbon are combusted to generate power and carbon dioxide-rich gas. The power is used to operate an air separation plant which provides the oxygen for the oxygen enrichment of the power or cogeneration plant. Additional nitrogen and/or steam produced may also be used to enhance oil recovery by placing these materials in an injection well either individually or in combination with the carbon dioxide-rich gas stream.
The combination of heat and carbon dioxide can further improve recovery and little carbon dioxide would be lost to the aqueous phase as a result.
Another means for producing the carbon dioxide is by injection of pure oxygen, oxygen-enriched air or air downhole. For wells that are sufficiently deep enough, the temperature will be sufficient to sustain combustion and produce carbon dioxide. For example, a 8000 foot deep well may have a temperature of 300OF which is hot enough to produce the carbon dioxide necessary for the enhanced oil recovery.
In a preferred embodiment of the present invention, a carbon dioxide nitrogen mixture with carbon dioxide present greater than 50% by volume is injected into the formation at or near the production well by optimizing the composition of the gas mixture. Due to the varied rates in the uptake of carbon dioxide and nitrogen, a near optimum composition can be maintained in the formation at that injection location. A second mixture of carbon dioxide and nitrogen would then be injected through injection well(s) located at a distance from the production well. The composition of this gas mixture would be such that the viscosity and surface tension of the oil is higher than that of the oil near or at the production well but still reduced in comparison to the untreated oil. Gas may be fed continuously to the injection well(s) or the well(s) can be shut for a period of at least a day to facilitate the uptake of the gas by the oil.
Oil is driven to the production well and fingering or bypass of the gas though the oil is minimized as a result. In this preferred embodiment, more than one remote injection point may be employed such that the viscosity and surface tension of the oil at the remote injection point becomes higher with each injection point further away from the well head injection point by optimizing the content of the carbon dioxide and nitrogen gas mixture.
Accordingly, the nitrogen content of the gas mixture will increase as one injects the mixture further from the production well. This gradient will result in a raising of carbon dioxide content above the 50% by volume as one injects at points getting sequentially closer to the production well. In this embodiment, a later possibly intermittent use of carbon dioxide flood, nitrogen flood or water flood to drive the oil to the production well would further improve yields.
A preferred composition for use in the methods of the present invention is that of at least 50% by volume carbon dioxide, the remainder being nitrogen or other inert gas including helium, argon or steam. In a more preferred embodiment, greater than 60% carbon dioxide by volume with the remainder being inert gases would comprise the gaseous mixture. In the most preferred embodiment, greater than 75% by volume of the gas mixture would be carbon dioxide and the remainder being inert gases.
In an additional embodiment, hydrocarbons can be added to the above described compositions. These hydrocarbons, such as methane, ethane and propane can come from traditional sources but may also come from the associated gas produced during oil production. The hydrocarbons can be separated from oil and reinjected into the ground or may be separated from oil and reinjected into the ground after burning a portion of the hydrocarbon in air, oxygen or oxygen enriched air.
EXAMPLES
Three model oils were studied to explore the potential of mixtures of carbon dioxide and nitrogen for enhanced oil recovery. A simulation was developed based on the Peng-Robinson equation of state for vapor-liquid 0io equilibrium, the Twu model for liquid phase viscosity and a modified form of the Brock and Bird equation for surface tension. The three oils employed in this study were of paraffin, naphthene and aromatic types. A gas mixture of carbon dioxide and nitrogen with a usage rate of 1 mole per mole of oil was presumed and a small quantity of water was added to the mixture since typically carbon dioxide flooding operations follow water flood procedures or are conducted as in the WAG method alternatively with waterflood. The quantity of water was based on 20% saturation for a typical oil. Pressures in the range of 1,500 psia to 2,500 psia and temperatures in the range of 75 0
F
to 200 0 F were studied.
As shown in Figs. 1, 2 and 3, and Tables 1, 2 and 3, the relationship of a paraffin, naphthene and aromatic oil viscosity at 75 0 F to the percentage of carbon dioxide in the oil recovery gas mixture is demonstrated. It can be seen that greater than 50% carbon dioxide in the gas mixture is advantageous in lowering the oil viscosity relative to the use of 100% carbon dioxide.
Table 1. Effect of CO2 Content of Gas on Paraffin Oil Viscosity at Various Pressures and 75 F CO2 Oil Oil Oil content of viscosity at viscosity at viscosity at gas 1500 psia 2000 psia 2500 psia (cP) (cP) (cP) 0 0.592 0.571 0.552 0.557 0.534 0.513 0.515 0.49 0.468 68 0.478 0.453 0.437 0.462 0.443 0.449 0.45 0.451 0.457 0.451 0.46 0.466 88 0.456 0.465 0.472 92 0.464 0.472 0.479 100 0.478 0.487 0.493 Table 2. Effect of CO2 Content of Gas on Naphthene Oil Viscosity at Various Pressures and 75 F CO2 Oil Oil Oil content of viscosity at viscosity at viscosity at gas 1500 psia 2000 psia 2500 psia (cP) (cP) (cP) 0 1.93 1.87 1.82 1.69 1.62 1.57 1.44 1.38 1.32 68 1.26 1.19 1.14 1.18 1.12 1.07 1.12 1.06 1.02 1.06 1.01 0.997 88 1.02 0.993 1.01 92 0.986 1.01 1.02 100 1.02 1.04 1.05 Table 3. Effect of C02 Content of Gas on Aromatic Oil Viscosity at Various Pressures and 75 F C02 Oil Oil Oil content of viscosity at viscosity at viscosity at gas 1500 psia 2000 psia 2500 psia (cP) (cP) (cP) 0 0.827 0.811 0.797 0.7566 0.738 0.722 0.679 0.658 0.642 68 0.615 0.595 0.578 0.587 0.567 0.552 0.566 0.547 0.532 0.544 0.526 0.512 88 0.529 0.512 0.519 92 0.51 0.52 0.527 100 0.527 0.537 0.544 Figs. 4, 5 and 6 and Tables 4, 5 and 6 show the relationship of a paraffin, naphthene and aromatic oil surface tension at 75 0 F to the percentage carbon dioxide and the oil recovery gas mixture for three different pressures. As can be seen in Figs. 4, 5 and 6, greater than 60% carbon dioxide in the gas mixture is advantageous in reducing surface tension in comparison to the use of pure carbon dioxide.
Table 4. Effect of CO2 Content of Gas on Paraffin Oil Surface Tension at Various Pressures and 75 F CO2 Oil surface Oil surface Oil surface content of tension at tension at tension at gas 1500 psia 2000 psia 2500 psia (dyne/cm) (dyne/cm) (dyne/cm) 0 19.22 18.39 17.65 17.1 16.19 15.41 14.93 13.99 13.21 68 13.27 12.35 11.8 12.59 11.86 11.86 12.09 11.91 11.9 11.96 11.95 11.95 88 11.98 11.98 11.98 92 12.02 12.02 12.02 100 12.09 12.1 12.1 Table 5. Effect of C02 Content of Gas on Naphthene Oil Surface Tension at Various Pressures and 75 F C02 Oil surface Oil surface Oil surface content of tension at tension at tension at gas 1500 psia 2000 psia 2500 psia (dyne/cm) (dyne/cm) (dyne/cm) 0 29.21 28.56 27.96 26.14 25.3 24.59 22.93 21.97 21.23 68 20.4 19.44 18.73 19.34 18.42 17.72 18.53 17.64 16.97 17.69 16.85 16.59 88 17.16 16.61 16.62 92 16.65 16.66 16.66 100 16.72 16.73 16.73 Table 6. Effect of CO2 Content of Gas on Aromatic Oil Surface Tension at Various Pressures and 75 F CO2 Oil surface Oil surface Oil surface content of tension at tension at tension at gas 1500 psia 2000 psia 2500 psia (dyne/cm) (dyne/cm) (dyne/cm) 0 29.84 29.29 28.79 26.71 25.96 25.33 23.41 22.53 21.87 68 20.81 19.94 19.28 19.73 18.87 18.25 18.92 18.08 17.48 18.06 17.28 16.72 88 17.52 16.77 16.76 92 16.8 16.8 16.8 100 16.86 16.86 16.86 Figs. 7 and 8 and Tables 7 and 8 show the relationship of a paraffin oil viscosity and surface tension at various temperatures to the percentage carbon dioxide and the oil recovery gas mixture. As demonstrated in the earlier examples, greater than 50% carbon dioxide in the gas mixture is advantageous in comparison to the use of pure carbon dioxide. Oil viscosity is greatly reduced at around 70 to 80% carbon dioxide while surface tension remains approximately constant at the higher carbon dioxide concentrations.
Table 7. Effect of CO2 Content of Gas on Paraffin Oil Viscosity at Various Temperatures and 2000 psia CO2 Oil Oil Oil Oil Oil content viscosity viscosity viscosity viscosity viscosity of gas at 75 F at 100 F at 125 F at 150 F at 200 F (cP) (cP) (cP) (cP) (cP) 0 0.571 0.486 0.419 0.365 0.282 0.49 0.429 0.375 0.329 0.257 0.443 0.387 0.341 0.301 0.235 0.451 0.394 0.342 0.298 0.229 0.46 0.402 0.348 0.304 0.23 88 0.465 0.407 0.352 0.307 0.233 92 0.472 0.413 0.358 0.312 0.237 100 0.487 0.426 0.369 0.321 0.244 Table 8. Effect of CO2 Content of Gas on Paraffin Oil Surface Tension at Various Temperatures and 2000 psia CO2 Oil Oil Oil Oil Oil content surface surface surface surface surface of gas tension tension tension tension tension at 75 F at 100 F at 125 F at 150 F at 200 F (dyne/cm) (dyne/cm) (dyne/cm) (dyne/cm) (dyne/cm) 0 18.39 17.3 16.21 15.13 13 13.99 12.91 12.29 11.63 10.26 11.86 10.53 10.06 9.582 8.574 11.91 10.52 9.887 9.265 8.167 11.95 10.52 9.888 9.266 8.044 88 11.98 10.52 9.887 9.266 8.046 92 12.02 10.52 9.888 9.266 8.044 100 12.1 10.52 9.887 9.265 8.045 Fig. 9 and Table 9 show the relationship of a paraffin oil relative to volume at various temperatures as to the percentage carbon dioxide in the oil recovery gas mixture. The relative volume is taken in comparison to a standard oil volume. Roughly 70% to 99% carbon dioxide in the gas mixture is advantageous in comparison to the use of pure carbon dioxide to maximize swelling in this case. As swelling of the oil increases, the oil will exit small pores within the subterranean formation and can be swept or driven to the production well by use of the various flood techniques.
Table 9. Effect of CO2 Content of Gas on Paraffin Oil Relative Volume at Various Temperatures and 2000 psia* 002 Oil Oil Oil Oil Oil content relative relative relative relative relative of gas volume volume volume volume volume at 75F at 100F at125F atl150F at 200F 0 1.036 1.053 1.071 1.090 1.131 1.118 1.135 1.154 1.176 1.235 1.193 1.222 1.244 1.27 1.353 1.188 1.217 1.249 1.287 1.392 1.183 1.211 1.243 1.280 1.398 88 1.179 1.207 1.239 1.276 1.391 92 1.175 1.203 1.234 1.271 1.383 100 1.167 1.194 1.224. 1.261 1.366 *Relative volume is in comparison to a standard oil volume While this invention has been described with respect to particular embodiments thereof, it is apparent that numerous other forms and modifications of the invention will be obvious to those skilled in the art. The appended claims of this invention generally should be construed to cover all such obvious forms and modifications which are within the true spirit and scope of the present invention.
Claims (39)
1. A method for enhancing the recovery of oil from an underground formation comprising injecting into said oil a gas mixture comprising at least by volume carbon dioxide.
2. The method as claimed in claim 1 wherein the remainder of said gas mixture is selected from the group consisting of an inert gas, mixtures of inert gases, hydrocarbons, steam, air or mixtures of these.
3. The method as claimed in claim 2 wherein said inert gas is selected from the group consisting of nitrogen, helium and argon.
4. The method as claimed in claim 1 wherein said gas mixture comprises greater than 60% by volume carbon dioxide.
The method as claimed in claim 1 wherein said gas mixture comprises greater than 70% carbon dioxide by volume.
6. The method as claimed in claim 1 wherein said gas mixture is injected into said oil at the well head.
7. The method as claimed in claim 1 wherein said gas mixture is injected into a single production well head.
8. The method as claimed in claim 7 wherein said injection is cyclical.
9. The method as claimed in claim 7 wherein said gas mixture is injected into an injection well different from said production well head.
The method as claimed in claim 9 wherein said gas mixture is injected in an alternating pattern with a driving fluid.
11. The method as claimed in claim 10 wherein said driving fluid is selected from the group consisting of steam, water, nitrogen, carbon dioxide and air.
12. The method as claimed in claim 9 wherein there are a plurality of different injection wells.
13. The method as claimed in claim 1 wherein said gas mixture is injected into said oil at a pressure ranging from about 100 psi to about 20,000 psi.
14. The method as claimed in claim 1 wherein said carbon dioxide is obtained from a power plant or co-generation plant or from in situ combustion through the injection of air, oxygen enriched air, or pure oxygen.
The method as claimed in claim 1 wherein said nitrogen is obtained from an air separation plant.
16. The method as claimed in claim 1 wherein after injection of said gas mixture said underground formation is sealed for at least one day.
17. The method as claimed in claim 16 wherein said sealed underground formation is opened and a flood of a material selected from the group consisting of carbon dioxide, nitrogen, water or brine is driven through said injection point.
18. A method for enhancing the recovery of oil from an underground formation comprising injecting into said oil a gas mixture comprising carbon dioxide and nitrogen wherein said carbon dioxide is present in said gas mixture in an amount of at least 50% by volume.
19. The method as claimed in claim 18 wherein said carbon dioxide is present in said gas mixture in an amount greater than 60% by volume.
The method as claimed in claim 18 wherein said carbon dioxide is present in said gas mixture in an amount greater than 70% by volume.
21. The method as claimed in claim 18 wherein said carbon dioxide is present in said gas mixture in an amount greater than 50% by volume and less than 99% by volume.
22. The method as claimed in claim 18 wherein said gas mixture is injected into said formation at a pressure of about 100 psi to about 20,000 psi.
23. The method as claimed in claim 18 wherein steam is additionally injected into said underground formation.
24. A method for enhancing the recovery of oil from an underground formation having at least one production well comprising injecting into said underground formation in at least two distinct injection points a gas mixture comprising carbon dioxide and nitrogen wherein said carbon dioxide is present in said gas mixture in an amount of at least 50% by volume at the first injection point and further wherein the volume percentage of nitrogen in said mixture is higher at said second injection point than said first injection point, and said first injection point is closer to said at least one production well than said second injection point.
The method as claimed in claim 24 wherein the volume percentage of nitrogen in said gas mixture increases at each injection point further from said production well.
26. The method as claimed in claim 24 wherein the viscosity and surface tension of said oil at said second injection point is higher than the surface tension and viscosity at said first injection point.
27. The method as claimed in claim 24 wherein said underground formation is sealed for at least one day.
28. The method as claimed in claim 27 wherein said underground formation is opened and flooded with a material selected from the group consisting of carbon dioxide, nitrogen, water and brine to improve oil recovery.
29. A method for lowering the viscosity and surface tension of oil in an underground formation comprising injecting the said oil a gas mixture comprising at least 50% by volume carbon dioxide.
The method as claimed in claim 29 wherein the remainder of said gas mixture is selected from the group consisting of an inert gas, mixtures of inert gases, hydrocarbons, steam, air or mixtures of these.
31. The method as claimed in claim 29 wherein said inert gas is selected from the group consisting of nitrogen, helium and argon.
32. The method as claimed in claim 29 wherein said gas mixture comprises at least 60% by volume carbon dioxide.
33. The method as claimed in claim 29 wherein said carbon dioxide comprises at least 70% by volume of said gas mixture.
34. The method as claimed in claim 29 wherein said gas mixture comprises about 50% to about 99% by volume carbon dioxide and about 1% to about 49% nitrogen by volume.
The method as claimed in claim 29 wherein said gas mixture is injected into said underground formation at a pressure of about 100 psi to about 20,000 psi.
36. The method as claimed in claim 29 wherein said hydrocarbons are derived from associated gas produced during the production of oil.
37. The method as claimed in claim 29 wherein said hydrocarbons are present in said mixture in an amount ranging from about 1% to about
38. A method for enhancing the recovery of oil substantially as herein described with reference to any one of the embodiments of the invention illustrated in the accompanying drawings and/or examples.
39. A method for lowering the viscosity and surface tension of oil substantially as herein described with reference to any one of the embodiments of the invention illustrated in the accompanying drawings and/or examples. DATED this 9th Day of May 2002 THE BOC GROUP, INC. Attorney: PAUL G HARRISON Fellow Institute of Patent Attorneys of Australia of BALDWIN SHELSTON WATERS
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US09/858,363 US20030037928A1 (en) | 2001-05-16 | 2001-05-16 | Enhanced oil recovery |
US09858363 | 2001-05-16 |
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AU40584/02A Abandoned AU4058402A (en) | 2001-05-16 | 2002-05-09 | Improved enhanced oil recovery |
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US (1) | US20030037928A1 (en) |
EP (1) | EP1258595A3 (en) |
CN (1) | CN1385595A (en) |
AU (1) | AU4058402A (en) |
CA (1) | CA2384612A1 (en) |
MX (1) | MXPA02004535A (en) |
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US7493952B2 (en) * | 2004-06-07 | 2009-02-24 | Archon Technologies Ltd. | Oilfield enhanced in situ combustion process |
GB2417739B (en) * | 2004-09-01 | 2006-07-26 | Statoil Asa | Method |
US9605522B2 (en) * | 2006-03-29 | 2017-03-28 | Pioneer Energy, Inc. | Apparatus and method for extracting petroleum from underground sites using reformed gases |
US7506685B2 (en) * | 2006-03-29 | 2009-03-24 | Pioneer Energy, Inc. | Apparatus and method for extracting petroleum from underground sites using reformed gases |
CA2891016C (en) * | 2007-02-10 | 2019-05-07 | Vast Power Portfolio, Llc | Hot fluid recovery of heavy oil with steam and carbon dioxide |
CN201031676Y (en) * | 2007-03-30 | 2008-03-05 | 辽河石油勘探局 | Boiler flue gas pressurization absorption CO2 gaseous state pouring well oil production device |
US8616294B2 (en) | 2007-05-20 | 2013-12-31 | Pioneer Energy, Inc. | Systems and methods for generating in-situ carbon dioxide driver gas for use in enhanced oil recovery |
US7650939B2 (en) * | 2007-05-20 | 2010-01-26 | Pioneer Energy, Inc. | Portable and modular system for extracting petroleum and generating power |
CN101126312B (en) * | 2007-08-17 | 2013-01-23 | 中国科学院武汉岩土力学研究所 | Fluctuation petroleum exploitation method |
US20090140444A1 (en) * | 2007-11-29 | 2009-06-04 | Total Separation Solutions, Llc | Compressed gas system useful for producing light weight drilling fluids |
US8450536B2 (en) | 2008-07-17 | 2013-05-28 | Pioneer Energy, Inc. | Methods of higher alcohol synthesis |
US7937948B2 (en) * | 2009-09-23 | 2011-05-10 | Pioneer Energy, Inc. | Systems and methods for generating electricity from carbonaceous material with substantially no carbon dioxide emissions |
CN101718192B (en) * | 2009-12-04 | 2012-07-18 | 北京高新利华催化材料制造有限公司 | Method for carrying out tertiary oil production on oil field |
CN102947412B (en) | 2010-06-04 | 2015-08-12 | 陶氏环球技术有限责任公司 | Recover the oil |
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US20130206403A1 (en) * | 2011-08-09 | 2013-08-15 | Stevan Jovanovic | Enhanced oil recovery process |
DE102011110213A1 (en) | 2011-08-16 | 2013-02-21 | Thyssenkrupp Uhde Gmbh | Method and device for recirculating exhaust gas from a gas turbine with subsequent waste heat boiler |
CN102392623B (en) * | 2011-10-31 | 2014-07-23 | 中国石油天然气股份有限公司 | Air-drive oil extraction method for low-permeability reservoir |
CN102606117B (en) * | 2012-04-05 | 2014-11-05 | 中国石油天然气股份有限公司 | Air nitrogen alternate flooding exploitation method for middle-deep low-permeability thin oil reservoir |
US9586827B2 (en) | 2013-09-06 | 2017-03-07 | David LeRoy Hagen | CO2 producing calciner |
CN104632158B (en) * | 2013-11-13 | 2017-02-08 | 中国石油化工股份有限公司 | Oil well response stage dividing and distinguishing method under carbon dioxide miscible displacement condition |
US10519757B2 (en) | 2016-02-09 | 2019-12-31 | Frank Thomas Graff, JR. | Multi-directional enhanced oil recovery (MEOR) method |
US10066469B2 (en) | 2016-02-09 | 2018-09-04 | Frank Thomas Graff | Multi-directional enhanced oil recovery (MEOR) method |
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EP3986596B1 (en) | 2019-08-23 | 2023-07-12 | John W. SCHULTES | Method and a direct reduction plant for producing direct reduced iron |
CN114427392A (en) * | 2020-09-29 | 2022-05-03 | 中国石油化工股份有限公司 | Method for exploiting heavy oil reservoir |
US20230112608A1 (en) | 2021-10-13 | 2023-04-13 | Disruptive Oil And Gas Technologies Corp | Nanobubble dispersions generated in electrochemically activated solutions |
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US2623596A (en) * | 1950-05-16 | 1952-12-30 | Atlantic Refining Co | Method for producing oil by means of carbon dioxide |
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2001
- 2001-05-16 US US09/858,363 patent/US20030037928A1/en not_active Abandoned
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- 2002-05-07 MX MXPA02004535A patent/MXPA02004535A/en unknown
- 2002-05-09 AU AU40584/02A patent/AU4058402A/en not_active Abandoned
- 2002-05-15 CN CN02120034A patent/CN1385595A/en active Pending
- 2002-05-15 EP EP02253397A patent/EP1258595A3/en not_active Withdrawn
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EP1258595A3 (en) | 2004-03-03 |
MXPA02004535A (en) | 2004-07-16 |
US20030037928A1 (en) | 2003-02-27 |
CA2384612A1 (en) | 2002-11-16 |
CN1385595A (en) | 2002-12-18 |
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