US3051235A - Recovery of petroleum crude oil, by in situ combustion and in situ hydrogenation - Google Patents
Recovery of petroleum crude oil, by in situ combustion and in situ hydrogenation Download PDFInfo
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- US3051235A US3051235A US717256A US71725658A US3051235A US 3051235 A US3051235 A US 3051235A US 717256 A US717256 A US 717256A US 71725658 A US71725658 A US 71725658A US 3051235 A US3051235 A US 3051235A
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- 238000002485 combustion reaction Methods 0.000 title description 21
- 239000003208 petroleum Substances 0.000 title description 17
- 238000011084 recovery Methods 0.000 title description 15
- 238000005984 hydrogenation reaction Methods 0.000 title description 14
- 238000011065 in-situ storage Methods 0.000 title description 12
- 239000010779 crude oil Substances 0.000 title description 4
- 239000003921 oil Substances 0.000 description 77
- 238000000034 method Methods 0.000 description 32
- 230000015572 biosynthetic process Effects 0.000 description 31
- 238000005755 formation reaction Methods 0.000 description 31
- 239000001257 hydrogen Substances 0.000 description 28
- 229910052739 hydrogen Inorganic materials 0.000 description 28
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 27
- 239000003054 catalyst Substances 0.000 description 27
- 238000002347 injection Methods 0.000 description 27
- 239000007924 injection Substances 0.000 description 27
- 238000004519 manufacturing process Methods 0.000 description 22
- 239000007789 gas Substances 0.000 description 16
- 239000012530 fluid Substances 0.000 description 14
- 239000000203 mixture Substances 0.000 description 11
- 238000006243 chemical reaction Methods 0.000 description 10
- 230000002000 scavenging effect Effects 0.000 description 7
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 6
- 239000001301 oxygen Substances 0.000 description 6
- 229910052760 oxygen Inorganic materials 0.000 description 6
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 4
- 239000011261 inert gas Substances 0.000 description 3
- 239000003027 oil sand Substances 0.000 description 3
- 239000011435 rock Substances 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 2
- 238000010793 Steam injection (oil industry) Methods 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 239000000567 combustion gas Substances 0.000 description 2
- 230000001276 controlling effect Effects 0.000 description 2
- 230000007423 decrease Effects 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 230000000149 penetrating effect Effects 0.000 description 2
- 239000002516 radical scavenger Substances 0.000 description 2
- 230000001105 regulatory effect Effects 0.000 description 2
- 238000009877 rendering Methods 0.000 description 2
- 238000012546 transfer Methods 0.000 description 2
- 229910000831 Steel Inorganic materials 0.000 description 1
- 241000364021 Tulsa Species 0.000 description 1
- 239000001569 carbon dioxide Substances 0.000 description 1
- 229910002092 carbon dioxide Inorganic materials 0.000 description 1
- 239000004568 cement Substances 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 238000006073 displacement reaction Methods 0.000 description 1
- 230000002349 favourable effect Effects 0.000 description 1
- 239000002737 fuel gas Substances 0.000 description 1
- 230000005484 gravity Effects 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- XMBWDFGMSWQBCA-UHFFFAOYSA-N hydrogen iodide Chemical compound I XMBWDFGMSWQBCA-UHFFFAOYSA-N 0.000 description 1
- 229910000043 hydrogen iodide Inorganic materials 0.000 description 1
- INQOMBQAUSQDDS-UHFFFAOYSA-N iodomethane Chemical compound IC INQOMBQAUSQDDS-UHFFFAOYSA-N 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 238000012423 maintenance Methods 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 239000003345 natural gas Substances 0.000 description 1
- 239000008239 natural water Substances 0.000 description 1
- PXHVJJICTQNCMI-UHFFFAOYSA-N nickel Substances [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 1
- 229910052759 nickel Inorganic materials 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 239000004058 oil shale Substances 0.000 description 1
- 230000035699 permeability Effects 0.000 description 1
- 239000012466 permeate Substances 0.000 description 1
- 238000004391 petroleum recovery Methods 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 239000000376 reactant Substances 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 239000004576 sand Substances 0.000 description 1
- 239000003566 sealing material Substances 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 239000010959 steel Substances 0.000 description 1
- 230000000153 supplemental effect Effects 0.000 description 1
- 230000001131 transforming effect Effects 0.000 description 1
Images
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
- E21B43/24—Enhanced recovery methods for obtaining hydrocarbons using heat, e.g. steam injection
- E21B43/243—Combustion in situ
Definitions
- This present invention generally relates to a method of recovering petroleum oil from a subterranean oil reservoir.
- the invention more particularly concerns a secondary recovery type procedure for producing oil, and it is especially adapted for use in reservoirs that contain relatively viscous oil.
- petroleum crude oils are hydrogenated in-situ within a reservoir by injecting hydrogen and a catalyst into the reservoir.
- Petroleum crude oil is generally recovered from an oil-bearing earth formation initially as a result of gas pressure, rock pressure, or natural water drive forcing the oil from the formation through a producing well to the surface. As oil production continues, the initial reservoir energy gradually decreases and finally becomes insulicient to force the oil to the production well. It is well known by the petroleum industry that a relatively small proportion of the oil in a subterranean oil reservoir is produced from the reservoir during this primary stage of production. It is also generally recognized that almost all reservoirs retain from about 30% to 90% of their original oil when they have ceased primary production; and it is not unusual for a reservoir containing highly viscous crude to retain at least 90% of the oil originally in place following primary production.
- Fluids which have been employed or suggested thus far as a scavenging media in oil recovery operations include gases such as natural gas, carbon dioxide, methane, iiue gas, and various hydrocarbons; and liquids such as water, petroleum fractions, aqueous sugar solutions, and the like.
- Methods that have appeared to be very attractive for the production of viscous oil are ones involving the use of scavenging iluids such as steam and hot combustion gases which heat up a reservoir, thereby reducing the viscosity of the oil Within the reservoir and rendering it much more mobile.
- the hot combustion gases may be generated by combustion processes conducted either outside or directly within a reservoir.
- the object of the present invention to provide an oil recovery method wherein highly viscous petroleum is readily recovered from subterranean reservoirs. More specifically, the object of this invention is a process for the in-situ hydrogenation of petroleum within a reservoir whereby the petroleum is made readily mobile and high recovery of the oil in place is obtained. It is especially an object of the invention to provide a method for petroleum recovery which is rapid and etlicient.
- the lirst step of the process lies in the injection of a mixture of a gaseous catalyst and hydrogen through an injection well into the reservoir.
- These materials as they are injected into the reservoir tend to ow through the reservoir in multiple flow paths. That is, the injected fluid tends to seek paths that are fingers through the reservoir extending from an injection well toward a production well.
- the operation in any given reservoir is carried out concurrently throughout the reservoir so that the multiple paths extend substantially throughout the reservoir.
- injection wells are preferably spaced in a pattern that covers the entire lateral extent of the reservoir in a -manner consistent with conventional Well patterns. In this Way, multiple Wells are provided from which the petroleum can be produced.
- the injection of the gaseous catalyst and hydrogen may be performed either sequentially or simultaneously.
- a mass of catalyst may be injected, followed by a mass of hydrogen-or an admixture of catalyst and hydrogen may be injected.
- the mass of hydrogen may be about 1% to 4% by Weight of the oil in place; and the mass of catalyst may be about 1% to 6% by Weight of the oil in place.
- hydrogen can be injected iirst and followed by the catalyst.
- the preferred method for the operation of this invention is the injection of a hydrogenating mixture of hydrogen and a gaseous catalyst such as methyl iodide, hydrogen iodide, or nickel carbonyl.
- This hydrogenating mixture can be injected continuously until ultimate oil recovery is obtained.
- the volume of hydrogen and catalyst be injected only at the beginning of the process and that it be limited to from about 1% to 10% by Weight of the oil in place.
- a supplemental driving or scavenging agent such as water or gas is then injected until ultimate oil recovery is obtained.
- the mass of the hydrogenating mixture serves to increase oil recovery beyond that obtainable by a conventional ⁇ water or gas drive operation.
- reservoir oil is hydrogenated in-situ at a temperature above 400 F. and generally Within the range of 400 F. and 1200 F. by direct contact between the oil and hydrogen in the presence of a catalyst.
- Suitable injection pressures are those above 50 pounds per square inch but not so great as to lift the overburden above the reservoir and thereby fracture the formations.
- the pressure required to lift the overburden is usually equal to about one pound per square inch per foot of depth and is usually referred to as the fracturing pressure.
- the process of this invention may be controlled in various ways.
- the rate of reaction of the process maybe readily adjusted and controlled by simply regulating the pressure Within a reservoir. High pressures tend to accelerate the rate of reaction; and, conversely, low pressures tend to retard the reaction.
- Controlling the pressu-re of a reservoir in the practice of this invention may be accomplished in eiect by regulating the relative rates of fluid injection and production.
- the pressure on any given reservoir may be readily controlled by simply controlling the back pressure on the production wells.
- the maximum pressure attainable is determined by the depth of the reservoir in question as well as the pressure of the fluids injected into the reservoir.
- the rate ⁇ at which catalyst and hydrogen are injected within a reservoir also has a bearing upon the rate at which the reactions of this invention take place.
- apparent rates of advance of the driving fluids of about one-tenth to one foot per day are usually employed.
- the hydrogen and catalyst be injected in a quantity and at a rate sucient to provide an apparent rate of advance through a reservoir of about one to two feet per day.
- Rates of advance of this magnitude assure lingering of the hydrogen and catalyst into the reservoir oil and thus promote their mixing and reaction with the oil.
- any scavenging agents subsequently injected advance through a reservoir at a rate less than one foot per day in order to maintainY an essentially bank-type displacement of uids from the reservoir.
- the hydrogen-containing gases and the catalysts used in this invention may be circulated repeatedly through a reservoir as may be necessary or desirable.
- a well bore penetrating an oil-bearing formation should be cased with pipe in a conventional manner whereby a mixture' of gaseous catalyst and hydrogen may be injected into the formation.
- Well bores laterally spaced from the injection borehole are also drilled as necesasry, and oil produced by the process is withdrawn from these wells.
- the mixture of catalyst and hydrogen is forced under pressure through the injection well into direct contact with the oil in the formation.
- the hydrogen permeates the oil thoroughly and produces-in the presence of the catalyst and by reaction with the reservoir-an upgraded oil.
- the upgraded oil has a lower specific gravity and viscosity than the original oil and is an excellent hydrogen-transfer agent. In other words, it tends to absorb hydrogen from injected gases and later release it to the reservoir oil.
- hydrogenation of the reservoir oil occurs by direct reaction with injected hydrogen and also by a transfer -mechanism involving oil previously hydrogenated.
- any driving fluid employed in the production of oil tends to select zones or fingers in traveling from an injection well to a production well. This is especially true when the driving or scavenging uid has a viscosity markedly lower than that of the driven fluid. In the present invention, this characteristic is -deliberately exploited so as to enhance the production of oil, since it promotes contact between the hydrogenating agents and viscous oil.
- the mobility of oil within a reservoir is by deiinition proportional to formation permeability and inversely proportional to the viscosity of the oil. Due to its increased mobility, the oil ows readily within the reservoir rock and drains into the production wells. The increased mobility also further promotes mixing of heated oil within the reservoir with unheated oil and with the injected gases.
- the reaction of this invention may be intiated within a reservoir by raising the temperature at the borehole face of the reservoir to reaction temperature. Any suitable means of supplying heat may be used. Preferred methods are those involving liberation of heat near the face of the yoil-productive formation.
- a borehole heater-activated by electrical energy or combustion products- may be placed in the well bore to preheat the reactants. Once initiated, the reaction sustains itself due to the heat supplied by the hydrogenation process.
- the accompanying drawing illustrates diagrammatically and in vertical section an oil reservoir and its relationship to the earths surface, and an oil production method as practiced according to this invention.
- the numeral 1 designates a subterranean oil-bearing formation, above which is a relatively impervious ⁇ stratum 2, and below which is another relatively impervious stratum 3. These impervious layers are usually lof a shale or other relatively impermeable composition.
- a well bore is drilled from the surface of the earth 4 -through the oil-bearing formationthis borehole being shown by the legend 5.
- a steel casing 6 is placed in the borehole and may terminate at the top of the oil sand.
- the annulus between the casing and borehole is sealed with cement or other sealing material in a conventional manner. The casing placed in this manner leaves a borehole within the oil sand which is completely unoased for the injection of fluids into the oilbearing formation.
- the casing may also be extended through the oil sand and, after being sealed in place, perforated by conventional means whereby an injected fluid will pass through the perforations into Ithe formation.
- control of the injection points for fluids into the formation may be eifected.
- perforations may be made in a selected part of the casing and lthe catalyst ⁇ hydrogen mixture thereby injected into a selected zone of the oil-bearing formation.
- -the injected uids are pumped through injection Well 7 into the productive formation, and oil production is realized through production Well 8.
- This well like injection well 7, is drilled from the surface of the earth through the productive sand formation as shown by the borehole 9.
- ia casing 10 is placed within the borehole and may lbe set at the top of the productive formation 1 or may extend through this formation and be perforated by conventional means.
- the annular space between borehole 9 and casing 10 may be cemented or sealed in a manner analogous to conventional oil eld practice.
- Another illustrative embodiment of this invention lies in a combination-type operation wherein the hydrogenation step of the invention is preceded by an in-situ combustion step.
- an inert gas such as nitrogen is injected into the reservoir to flush oxygen from the vicinity of the injection Well.
- quantities of hydrogen and gaseous hydrogenation catalyst are injected into the reservoir in the manner described hereinfbefore so as to effect hydrogenation of the oil in place.
- a scavenging duid may be injected after -the hydrogen and catalyst, also as described hereinbefore.
- the in-situ combustion step described ⁇ above achieves several desirable objectives. First, it heats up a substantial portion -of the reservoir and brings it up to a temperature favorable to the hydrogenation step which fol- !lows. Second, it reduces the viscosity of the oil in place, thereby rendering the oil much more mobile and readily contacted by the hydrogenating gases and catalyst.
- the in-situ combustion step may make use of any conventional technique of this type.
- a combustible mixture of fuel gas and oxygen may be passed ⁇ down an injection Well bore.
- the combustible mix-ture may then be ignited and its heat of combustion used to start the combustion of part of the oil within the surrounding formation.
- Injection of the combustible mixture may then be suspended and oxygen alone supplied to move the combustion front away from the injection borehole.
- the injection of an inert gas followed by the injection of hydrogen and a gaseous hydrogenation catalyst may be practiced as described hereinabove.
- the combustion front need not penetrate Within a formation much more than 20 to 40 feet to achieve the objects -of the in-situ combustion step. It will also be noted that the in-situ combustion step may be used to help build up the pressure of the reservoir to whatever level is desired. The combustion process Will tend to generate large volumes of gas which may be held within the reservoir by simply keeping the production wells shut dow-n.
- a method of producing petroleum crude oil from a subterranean oil bearing formation which comprises injecting ⁇ an oxygen-containing gas into the formation through an input well under conditions to effect combustion within a zone of the formation adjacent said input well, continuing said injection of oxygen-containing gas until the temperature within said zone is between 400 F.
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- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Geology (AREA)
- Mining & Mineral Resources (AREA)
- Physics & Mathematics (AREA)
- Environmental & Geological Engineering (AREA)
- Fluid Mechanics (AREA)
- General Life Sciences & Earth Sciences (AREA)
- Geochemistry & Mineralogy (AREA)
- Production Of Liquid Hydrocarbon Mixture For Refining Petroleum (AREA)
Description
Aug. 28, 1962 PRODUCED OIL INJECTED FLUIDS w. P. BANKS 3,051,235 RECOVERY oF PETROLEUM CRUDE on. BY 1N sITU COMBUSTION AND 1N sITU HYDROGENATION Filed Feb. 24, 1958 Byw. Attorney 3,05l,235 Patented Aug. 28, 1962 ice 3,051,235 RECOVERY F PETROLEUM CRUDE GIL, BY
1N SlTU CMBUSTION AND IN SITU HY- DROGENATIUN William P. Banks, Tulsa, Okla., assignor, by mesne assignments, to Jersey Production Research Company Filed Feb. 24, 1958, Ser. No. 717,256 1 Claim. (Cl. 166-11) This present invention generally relates to a method of recovering petroleum oil from a subterranean oil reservoir. The invention more particularly concerns a secondary recovery type procedure for producing oil, and it is especially adapted for use in reservoirs that contain relatively viscous oil. In accordance with this invention, petroleum crude oils are hydrogenated in-situ within a reservoir by injecting hydrogen and a catalyst into the reservoir.
Petroleum crude oil is generally recovered from an oil-bearing earth formation initially as a result of gas pressure, rock pressure, or natural water drive forcing the oil from the formation through a producing well to the surface. As oil production continues, the initial reservoir energy gradually decreases and finally becomes insulicient to force the oil to the production well. It is well known by the petroleum industry that a relatively small proportion of the oil in a subterranean oil reservoir is produced from the reservoir during this primary stage of production. It is also generally recognized that almost all reservoirs retain from about 30% to 90% of their original oil when they have ceased primary production; and it is not unusual for a reservoir containing highly viscous crude to retain at least 90% of the oil originally in place following primary production.
It has, accordingly, been a continuing problem and object in the petroleum industry to recover the large amounts of oil that remain within a reservoir following primary production. Numerous methods have been suggested or employed to date for this purpose. In general, the methods used have involved injecting a scavenging iiuid into a reservoir through one or more injection wells and thereby displacing the oil from the reservoir through one or more spaced production wells. Fluids which have been employed or suggested thus far as a scavenging media in oil recovery operations include gases such as natural gas, carbon dioxide, methane, iiue gas, and various hydrocarbons; and liquids such as water, petroleum fractions, aqueous sugar solutions, and the like. Unfortunately, none of these procedures are markedly eiective in recovering a heavy viscous oil from a reservoir. The primary reason that these methods have not proved themselves of value in the production of Viscous crudes is the high capillary resistance Within the interstices of reservoir rocks to the iiow of viscous oil.
Methods that have appeared to be very attractive for the production of viscous oil are ones involving the use of scavenging iluids such as steam and hot combustion gases which heat up a reservoir, thereby reducing the viscosity of the oil Within the reservoir and rendering it much more mobile. The hot combustion gases may be generated by combustion processes conducted either outside or directly within a reservoir.
While methods of heating a reservoir for scavenging oil from the reservoir have been recognized to possess very desirable advantages, they have also been recognized to have serious disadvantages. For example, in the case of combustion processes, it is diiiicult to regulate and maintain a combustion front throughout a reservoir. Frequently, the combustion process is interrupted and the llame front disappears-all too often necessitating abandonment of the operation.
In the case of steam-injection processes, it has been found that such processes are very slow; and they take very long periods of time for the steam to effectively penetrate and raise the temperature of a reservoir. Furthermore, when the pressure of the steam is increased in an effort to speed up the recovery process, the accompanying rise in the temperature of the steam causes large amounts of heat to be lost to the surrounding formations in which oil is not present. Even at low operating pressures, heat losses in a steam injection process are undesirably high-thereby tending to make this type of operation inefficient and uneconomical.
Accordingly, it is an object of the present invention to provide an oil recovery method wherein highly viscous petroleum is readily recovered from subterranean reservoirs. More specifically, the object of this invention is a process for the in-situ hydrogenation of petroleum within a reservoir whereby the petroleum is made readily mobile and high recovery of the oil in place is obtained. It is especially an object of the invention to provide a method for petroleum recovery which is rapid and etlicient. These and related objects of this invention Will become more apparent from the ensuing description.
In the process of this invention, petroleum is hydrogenated within a reservoir so that an enhancement of its recovery is realized. The lirst step of the process lies in the injection of a mixture of a gaseous catalyst and hydrogen through an injection well into the reservoir. These materials as they are injected into the reservoir tend to ow through the reservoir in multiple flow paths. That is, the injected fluid tends to seek paths that are fingers through the reservoir extending from an injection well toward a production well. Preferably, the operation in any given reservoir is carried out concurrently throughout the reservoir so that the multiple paths extend substantially throughout the reservoir. Thus, injection wells are preferably spaced in a pattern that covers the entire lateral extent of the reservoir in a -manner consistent with conventional Well patterns. In this Way, multiple Wells are provided from which the petroleum can be produced.
The injection of the gaseous catalyst and hydrogen may be performed either sequentially or simultaneously. For example, a mass of catalyst may be injected, followed by a mass of hydrogen-or an admixture of catalyst and hydrogen may be injected. The mass of hydrogen may be about 1% to 4% by Weight of the oil in place; and the mass of catalyst may be about 1% to 6% by Weight of the oil in place.
In the operation of this process, hydrogen can be injected iirst and followed by the catalyst. However, the preferred method for the operation of this invention is the injection of a hydrogenating mixture of hydrogen and a gaseous catalyst such as methyl iodide, hydrogen iodide, or nickel carbonyl. This hydrogenating mixture can be injected continuously until ultimate oil recovery is obtained. However, it is preferred that the volume of hydrogen and catalyst be injected only at the beginning of the process and that it be limited to from about 1% to 10% by Weight of the oil in place. A supplemental driving or scavenging agent such as water or gas is then injected until ultimate oil recovery is obtained. The mass of the hydrogenating mixture serves to increase oil recovery beyond that obtainable by a conventional `water or gas drive operation.
In the process of this invention, reservoir oil is hydrogenated in-situ at a temperature above 400 F. and generally Within the range of 400 F. and 1200 F. by direct contact between the oil and hydrogen in the presence of a catalyst. Suitable injection pressures are those above 50 pounds per square inch but not so great as to lift the overburden above the reservoir and thereby fracture the formations. The pressure required to lift the overburden is usually equal to about one pound per square inch per foot of depth and is usually referred to as the fracturing pressure. Structural limitations of shallow petroleum formations--Such as shallow oil sands, tar sands, and oil shale deposits-usually require the maintenance of relatively low pressures, since Athe higher pressures tend to create fractures in the formation extending into the overburden. These fractures in turn permit undesirable leakage of fluids from the oil-bearing formations into adjacent structures.
The process of this invention may be controlled in various ways. In general, the rate of reaction of the process maybe readily adjusted and controlled by simply regulating the pressure Within a reservoir. High pressures tend to accelerate the rate of reaction; and, conversely, low pressures tend to retard the reaction.
Controlling the pressu-re of a reservoir in the practice of this invention may be accomplished in eiect by regulating the relative rates of fluid injection and production. Thus, it will be apparent that the pressure on any given reservoir may be readily controlled by simply controlling the back pressure on the production wells. The maximum pressure attainable, of course, is determined by the depth of the reservoir in question as well as the pressure of the fluids injected into the reservoir.
Other conditions being fixed, the rate `at which catalyst and hydrogen are injected within a reservoir also has a bearing upon the rate at which the reactions of this invention take place. In this connection, it is desirable that the hydrogen and catalyst-and any scavenging agentsbe passed through a reservoir at a rate suicient to stimulate intimate mixing and contacting. In conventional oil recovery processes (e.g., conventional gas and water drives), apparent rates of advance of the driving fluids of about one-tenth to one foot per day are usually employed. In the practice of this invention, however, it is preferred that the hydrogen and catalyst be injected in a quantity and at a rate sucient to provide an apparent rate of advance through a reservoir of about one to two feet per day. Rates of advance of this magnitude assure lingering of the hydrogen and catalyst into the reservoir oil and thus promote their mixing and reaction with the oil. Once the hydrogen and catalyst have been injected, it is generally preferred that any scavenging agents subsequently injected advance through a reservoir at a rate less than one foot per day in order to maintainY an essentially bank-type displacement of uids from the reservoir. It will be recognized, of course, that the hydrogen-containing gases and the catalysts used in this invention may be circulated repeatedly through a reservoir as may be necessary or desirable.
In carrying out the present process, a well bore penetrating an oil-bearing formation should be cased with pipe in a conventional manner whereby a mixture' of gaseous catalyst and hydrogen may be injected into the formation. Well bores laterally spaced from the injection borehole are also drilled as necesasry, and oil produced by the process is withdrawn from these wells. The mixture of catalyst and hydrogen is forced under pressure through the injection well into direct contact with the oil in the formation. The hydrogen permeates the oil thoroughly and produces-in the presence of the catalyst and by reaction with the reservoir-an upgraded oil. The upgraded oil has a lower specific gravity and viscosity than the original oil and is an excellent hydrogen-transfer agent. In other words, it tends to absorb hydrogen from injected gases and later release it to the reservoir oil. Thus, hydrogenation of the reservoir oil occurs by direct reaction with injected hydrogen and also by a transfer -mechanism involving oil previously hydrogenated.
In addition to this upgrading phenomenon, several other actions occur in the process of the invention which further promote oil recovery. For example, as beforementioned, any driving fluid employed in the production of oil tends to select zones or fingers in traveling from an injection well to a production well. This is especially true when the driving or scavenging uid has a viscosity markedly lower than that of the driven fluid. In the present invention, this characteristic is -deliberately exploited so as to enhance the production of oil, since it promotes contact between the hydrogenating agents and viscous oil.
`As the hydrogen and catalyst in a process of this invention finger through a reservoir-and as hydrogenation takes place, transforming viscous petroleum to products of lower viscosity-heat released by the hydrogenation is transmitted through the reservoir, thereby further reducing the viscosity of the oil substantially. As the viscosity of the oil decreases, its mobility within the reservoir rapidly increases. The mobility of oil within a reservoir is by deiinition proportional to formation permeability and inversely proportional to the viscosity of the oil. Due to its increased mobility, the oil ows readily within the reservoir rock and drains into the production wells. The increased mobility also further promotes mixing of heated oil within the reservoir with unheated oil and with the injected gases.
The injected hydrogen and catalyst gases and the oil as it is hydrogenated tend to move up-structure in a reservoir, while the heavier reservoir fluids tend to ow downward. In other words, the low-density materials-hydrogen, gaseous catalyst, and hydrogenated oil-tend to diffuse upward through the denser reservoir oil. An eflicient contacting and mixing system is thus provided which further enhances oil hydrogenation.
The reaction of this invention may be intiated within a reservoir by raising the temperature at the borehole face of the reservoir to reaction temperature. Any suitable means of supplying heat may be used. Preferred methods are those involving liberation of heat near the face of the yoil-productive formation. A borehole heater-activated by electrical energy or combustion products-may be placed in the well bore to preheat the reactants. Once initiated, the reaction sustains itself due to the heat supplied by the hydrogenation process.
Insofar as injection or flooding patterns are concerned, it should be noted that any conventional flooding program used in the recovery of oil such as linear, 4-spot, S-spot, and related flooding patterns may be employed. Olbviously, in these patterns it will be understood that the wells conventionally designated `as injection and production wells will be similarly employed in carrying out the present process. The process of this invention is illustrated diagramrnatically by the accompanying drawing.
The accompanying drawing illustrates diagrammatically and in vertical section an oil reservoir and its relationship to the earths surface, and an oil production method as practiced according to this invention.
With reference to the drawing, the numeral 1 designates a subterranean oil-bearing formation, above which is a relatively impervious `stratum 2, and below which is another relatively impervious stratum 3. These impervious layers are usually lof a shale or other relatively impermeable composition. A well bore is drilled from the surface of the earth 4 -through the oil-bearing formationthis borehole being shown by the legend 5. A steel casing 6 is placed in the borehole and may terminate at the top of the oil sand. The annulus between the casing and borehole is sealed with cement or other sealing material in a conventional manner. The casing placed in this manner leaves a borehole within the oil sand which is completely unoased for the injection of fluids into the oilbearing formation.
As in conventional oil field practice, the casing may also be extended through the oil sand and, after being sealed in place, perforated by conventional means whereby an injected fluid will pass through the perforations into Ithe formation. By using this technique of placing the casing and then perforating the casing at desired points, control of the injection points for fluids into the formation may be eifected. For example, perforations may be made in a selected part of the casing and lthe catalyst` hydrogen mixture thereby injected into a selected zone of the oil-bearing formation. This and other obvious procedures may be practiced without departing from the scope of this invention.
As beforementioned, -the injected uids are pumped through injection Well 7 into the productive formation, and oil production is realized through production Well 8. This well, like injection well 7, is drilled from the surface of the earth through the productive sand formation as shown by the borehole 9. Here again ia casing 10 is placed within the borehole and may lbe set at the top of the productive formation 1 or may extend through this formation and be perforated by conventional means. The annular space between borehole 9 and casing 10 may be cemented or sealed in a manner analogous to conventional oil eld practice.
As may be noted, the Ysurface equipment which would normally be employed in injecting or producing fluids via Wells penetrating an oil reservoir is not shown. The inclusion of such equipment is not considered essential for the purpose of describing this invention.
Another illustrative embodiment of this invention lies in a combination-type operation wherein the hydrogenation step of the invention is preceded by an in-situ combustion step. After the in-situ combustion reaction has proceeded a substantial preselected distance within a reservoir from an injection well, an inert gas such as nitrogen is injected into the reservoir to flush oxygen from the vicinity of the injection Well. Thereafter, quantities of hydrogen and gaseous hydrogenation catalyst are injected into the reservoir in the manner described hereinfbefore so as to effect hydrogenation of the oil in place. A scavenging duid may be injected after -the hydrogen and catalyst, also as described hereinbefore.
The in-situ combustion step described `above achieves several desirable objectives. First, it heats up a substantial portion -of the reservoir and brings it up to a temperature favorable to the hydrogenation step which fol- !lows. Second, it reduces the viscosity of the oil in place, thereby rendering the oil much more mobile and readily contacted by the hydrogenating gases and catalyst.
The in-situ combustion step may make use of any conventional technique of this type. For example, it is contemplated that a combustible mixture of fuel gas and oxygen may be passed `down an injection Well bore. The combustible mix-ture may then be ignited and its heat of combustion used to start the combustion of part of the oil within the surrounding formation. Injection of the combustible mixture may then be suspended and oxygen alone supplied to move the combustion front away from the injection borehole. When the combustion front has proceeded an adequate predetermined distance into the formation, the injection of an inert gas followed by the injection of hydrogen and a gaseous hydrogenation catalyst may be practiced as described hereinabove. Generally speaking, the combustion front need not penetrate Within a formation much more than 20 to 40 feet to achieve the objects -of the in-situ combustion step. It will also be noted that the in-situ combustion step may be used to help build up the pressure of the reservoir to whatever level is desired. The combustion process Will tend to generate large volumes of gas which may be held within the reservoir by simply keeping the production wells shut dow-n.
The invention claimed is:
A method of producing petroleum crude oil from a subterranean oil bearing formation which comprises injecting `an oxygen-containing gas into the formation through an input well under conditions to effect combustion within a zone of the formation adjacent said input well, continuing said injection of oxygen-containing gas until the temperature within said zone is between 400 F. and 1200" F., thereafter discontinuing the injection of said oxygen-containing gas to terminate said combustion, injecting an inert gas Within said formation through said input well to flush said oxygen-containi-ng gas from said zone adjacent s-aid input well, then injecting hydrogen and a gaseous hydrogenation catalyst within the formation through said input Well whereby to hydrogenate oil within the formation in the presence of said catalyst, maintaining the pressure `of the formation in excess of 50 p.s.i.g., and recovering oil from the formation through an output well laterally spaced from said input well.
References Cited in the file of this patent UNITED STATES PATENTS 1,457,479 Walcott June 5, 1923 2,412,765 Buddrus et al Dec. 17, 1946 2,595,979 Pevere et al May 6, 1952 2,689,252 Clark Sept. 14, 1954 2,768,121 Denton et al. Oct. 23, 1956 2,788,071 Pelzer Apr. 9, 1957 2,857,002 Pevere et al. Oct. 21, 1958 FOREIGN PATENTS 696,524 Great Britain June 6, 1951
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US717256A US3051235A (en) | 1958-02-24 | 1958-02-24 | Recovery of petroleum crude oil, by in situ combustion and in situ hydrogenation |
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US717256A US3051235A (en) | 1958-02-24 | 1958-02-24 | Recovery of petroleum crude oil, by in situ combustion and in situ hydrogenation |
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Cited By (51)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3102588A (en) * | 1959-07-24 | 1963-09-03 | Phillips Petroleum Co | Process for recovering hydrocarbon from subterranean strata |
US3156299A (en) * | 1963-01-07 | 1964-11-10 | Phillips Petroleum Co | Subterranean chemical process |
US3208514A (en) * | 1962-10-31 | 1965-09-28 | Continental Oil Co | Recovery of hydrocarbons by in-situ hydrogenation |
US3327782A (en) * | 1962-09-10 | 1967-06-27 | Pan American Petroleum Corp | Underground hydrogenation of oil |
US3457996A (en) * | 1968-07-30 | 1969-07-29 | Phillips Petroleum Co | Thermal oil recovery process utilizing decomposition of co |
US3598182A (en) * | 1967-04-25 | 1971-08-10 | Justheim Petroleum Co | Method and apparatus for in situ distillation and hydrogenation of carbonaceous materials |
US3766982A (en) * | 1971-12-27 | 1973-10-23 | Justheim Petrol Co | Method for the in-situ treatment of hydrocarbonaceous materials |
US4183405A (en) * | 1978-10-02 | 1980-01-15 | Magnie Robert L | Enhanced recoveries of petroleum and hydrogen from underground reservoirs |
US4186800A (en) * | 1978-01-23 | 1980-02-05 | Texaco Inc. | Process for recovering hydrocarbons |
US4241790A (en) * | 1979-05-14 | 1980-12-30 | Magnie Robert L | Recovery of crude oil utilizing hydrogen |
US4444257A (en) * | 1980-12-12 | 1984-04-24 | Uop Inc. | Method for in situ conversion of hydrocarbonaceous oil |
US4597441A (en) * | 1984-05-25 | 1986-07-01 | World Energy Systems, Inc. | Recovery of oil by in situ hydrogenation |
US4691771A (en) * | 1984-09-25 | 1987-09-08 | Worldenergy Systems, Inc. | Recovery of oil by in-situ combustion followed by in-situ hydrogenation |
US5054551A (en) * | 1990-08-03 | 1991-10-08 | Chevron Research And Technology Company | In-situ heated annulus refining process |
US5105887A (en) * | 1991-02-28 | 1992-04-21 | Union Oil Company Of California | Enhanced oil recovery technique using hydrogen precursors |
US6016868A (en) * | 1998-06-24 | 2000-01-25 | World Energy Systems, Incorporated | Production of synthetic crude oil from heavy hydrocarbons recovered by in situ hydrovisbreaking |
US6016867A (en) * | 1998-06-24 | 2000-01-25 | World Energy Systems, Incorporated | Upgrading and recovery of heavy crude oils and natural bitumens by in situ hydrovisbreaking |
US20040140096A1 (en) * | 2002-10-24 | 2004-07-22 | Sandberg Chester Ledlie | Insulated conductor temperature limited heaters |
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US20050269093A1 (en) * | 2004-04-23 | 2005-12-08 | Sandberg Chester L | Variable frequency temperature limited heaters |
US7225866B2 (en) | 2001-04-24 | 2007-06-05 | Shell Oil Company | In situ thermal processing of an oil shale formation using a pattern of heat sources |
US20070137857A1 (en) * | 2005-04-22 | 2007-06-21 | Vinegar Harold J | Low temperature monitoring system for subsurface barriers |
US20070278344A1 (en) * | 2006-06-06 | 2007-12-06 | Pioneer Invention, Inc. D/B/A Pioneer Astronautics | Apparatus and Method for Producing Lift Gas and Uses Thereof |
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US20080283247A1 (en) * | 2007-05-20 | 2008-11-20 | Zubrin Robert M | Portable and modular system for extracting petroleum and generating power |
US20080283249A1 (en) * | 2007-05-19 | 2008-11-20 | Zubrin Robert M | Apparatus, methods, and systems for extracting petroleum using a portable coal reformer |
US7461691B2 (en) | 2001-10-24 | 2008-12-09 | Shell Oil Company | In situ recovery from a hydrocarbon containing formation |
US7533719B2 (en) | 2006-04-21 | 2009-05-19 | Shell Oil Company | Wellhead with non-ferromagnetic materials |
US7540324B2 (en) | 2006-10-20 | 2009-06-02 | Shell Oil Company | Heating hydrocarbon containing formations in a checkerboard pattern staged process |
US7549470B2 (en) | 2005-10-24 | 2009-06-23 | Shell Oil Company | Solution mining and heating by oxidation for treating hydrocarbon containing formations |
US20090236093A1 (en) * | 2006-03-29 | 2009-09-24 | Pioneer Energy, Inc. | Apparatus and Method for Extracting Petroleum from Underground Sites Using Reformed Gases |
US20100088951A1 (en) * | 2008-07-17 | 2010-04-15 | Pioneer Astronautics | Novel Methods of Higher Alcohol Synthesis |
US7798221B2 (en) | 2000-04-24 | 2010-09-21 | Shell Oil Company | In situ recovery from a hydrocarbon containing formation |
US7798220B2 (en) | 2007-04-20 | 2010-09-21 | Shell Oil Company | In situ heat treatment of a tar sands formation after drive process treatment |
US7831133B2 (en) | 2005-04-22 | 2010-11-09 | Shell Oil Company | Insulated conductor temperature limited heater for subsurface heating coupled in a three-phase WYE configuration |
US20100314136A1 (en) * | 2007-05-20 | 2010-12-16 | Zubrin Robert M | Systems and methods for generating in-situ carbon dioxide driver gas for use in enhanced oil recovery |
US7866388B2 (en) | 2007-10-19 | 2011-01-11 | Shell Oil Company | High temperature methods for forming oxidizer fuel |
US20110203292A1 (en) * | 2009-09-23 | 2011-08-25 | Pioneer Energy Inc. | Methods for generating electricity from carbonaceous material with substantially no carbon dioxide emissions |
US8151907B2 (en) | 2008-04-18 | 2012-04-10 | Shell Oil Company | Dual motor systems and non-rotating sensors for use in developing wellbores in subsurface formations |
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US8327932B2 (en) | 2009-04-10 | 2012-12-11 | Shell Oil Company | Recovering energy from a subsurface formation |
US20130161008A1 (en) * | 2011-12-22 | 2013-06-27 | Argonne National Laboratory | Preparation and use of nano-catalysts for in-situ reaction with kerogen |
US8602095B2 (en) | 2006-03-29 | 2013-12-10 | Pioneer Energy, Inc. | Apparatus and method for extracting petroleum from underground sites using reformed gases |
US8631866B2 (en) | 2010-04-09 | 2014-01-21 | Shell Oil Company | Leak detection in circulated fluid systems for heating subsurface formations |
US8691253B1 (en) * | 2008-05-28 | 2014-04-08 | Rhonda Tracy | Shark repellent |
US8701768B2 (en) | 2010-04-09 | 2014-04-22 | Shell Oil Company | Methods for treating hydrocarbon formations |
US8820406B2 (en) | 2010-04-09 | 2014-09-02 | Shell Oil Company | Electrodes for electrical current flow heating of subsurface formations with conductive material in wellbore |
US9016370B2 (en) | 2011-04-08 | 2015-04-28 | Shell Oil Company | Partial solution mining of hydrocarbon containing layers prior to in situ heat treatment |
US9033042B2 (en) | 2010-04-09 | 2015-05-19 | Shell Oil Company | Forming bitumen barriers in subsurface hydrocarbon formations |
US9309755B2 (en) | 2011-10-07 | 2016-04-12 | Shell Oil Company | Thermal expansion accommodation for circulated fluid systems used to heat subsurface formations |
US10047594B2 (en) | 2012-01-23 | 2018-08-14 | Genie Ip B.V. | Heater pattern for in situ thermal processing of a subsurface hydrocarbon containing formation |
Citations (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US1457479A (en) * | 1920-01-12 | 1923-06-05 | Edson R Wolcott | Method of increasing the yield of oil wells |
US2412765A (en) * | 1941-07-25 | 1946-12-17 | Phillips Petroleum Co | Recovery of hydrocarbons |
US2595979A (en) * | 1949-01-25 | 1952-05-06 | Texas Co | Underground liquefaction of coal |
GB696524A (en) * | 1950-07-27 | 1953-09-02 | Stanolind Oil & Gas Co | Improvements in or relating to recovery of oil from reservoirs |
US2689252A (en) * | 1949-11-28 | 1954-09-14 | Phillips Petroleum Co | Hydrocarbon synth esis and catalyst therefor |
US2768121A (en) * | 1954-11-18 | 1956-10-23 | Socony Mobil Oil Co Inc | Treatment of hydrocarbons with iodine and/or hydrogen iodide followed by hydrogenation |
US2788071A (en) * | 1954-03-05 | 1957-04-09 | Sinclair Oil & Gas Company | Oil recovery process |
US2857002A (en) * | 1956-03-19 | 1958-10-21 | Texas Co | Recovery of viscous crude oil |
-
1958
- 1958-02-24 US US717256A patent/US3051235A/en not_active Expired - Lifetime
Patent Citations (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US1457479A (en) * | 1920-01-12 | 1923-06-05 | Edson R Wolcott | Method of increasing the yield of oil wells |
US2412765A (en) * | 1941-07-25 | 1946-12-17 | Phillips Petroleum Co | Recovery of hydrocarbons |
US2595979A (en) * | 1949-01-25 | 1952-05-06 | Texas Co | Underground liquefaction of coal |
US2689252A (en) * | 1949-11-28 | 1954-09-14 | Phillips Petroleum Co | Hydrocarbon synth esis and catalyst therefor |
GB696524A (en) * | 1950-07-27 | 1953-09-02 | Stanolind Oil & Gas Co | Improvements in or relating to recovery of oil from reservoirs |
US2788071A (en) * | 1954-03-05 | 1957-04-09 | Sinclair Oil & Gas Company | Oil recovery process |
US2768121A (en) * | 1954-11-18 | 1956-10-23 | Socony Mobil Oil Co Inc | Treatment of hydrocarbons with iodine and/or hydrogen iodide followed by hydrogenation |
US2857002A (en) * | 1956-03-19 | 1958-10-21 | Texas Co | Recovery of viscous crude oil |
Cited By (205)
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---|---|---|---|---|
US3102588A (en) * | 1959-07-24 | 1963-09-03 | Phillips Petroleum Co | Process for recovering hydrocarbon from subterranean strata |
US3327782A (en) * | 1962-09-10 | 1967-06-27 | Pan American Petroleum Corp | Underground hydrogenation of oil |
US3208514A (en) * | 1962-10-31 | 1965-09-28 | Continental Oil Co | Recovery of hydrocarbons by in-situ hydrogenation |
US3156299A (en) * | 1963-01-07 | 1964-11-10 | Phillips Petroleum Co | Subterranean chemical process |
US3598182A (en) * | 1967-04-25 | 1971-08-10 | Justheim Petroleum Co | Method and apparatus for in situ distillation and hydrogenation of carbonaceous materials |
US3457996A (en) * | 1968-07-30 | 1969-07-29 | Phillips Petroleum Co | Thermal oil recovery process utilizing decomposition of co |
US3766982A (en) * | 1971-12-27 | 1973-10-23 | Justheim Petrol Co | Method for the in-situ treatment of hydrocarbonaceous materials |
US4186800A (en) * | 1978-01-23 | 1980-02-05 | Texaco Inc. | Process for recovering hydrocarbons |
US4183405A (en) * | 1978-10-02 | 1980-01-15 | Magnie Robert L | Enhanced recoveries of petroleum and hydrogen from underground reservoirs |
US4241790A (en) * | 1979-05-14 | 1980-12-30 | Magnie Robert L | Recovery of crude oil utilizing hydrogen |
US4444257A (en) * | 1980-12-12 | 1984-04-24 | Uop Inc. | Method for in situ conversion of hydrocarbonaceous oil |
US4597441A (en) * | 1984-05-25 | 1986-07-01 | World Energy Systems, Inc. | Recovery of oil by in situ hydrogenation |
US4691771A (en) * | 1984-09-25 | 1987-09-08 | Worldenergy Systems, Inc. | Recovery of oil by in-situ combustion followed by in-situ hydrogenation |
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US20090071647A1 (en) * | 2003-04-24 | 2009-03-19 | Vinegar Harold J | Thermal processes for subsurface formations |
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US7793722B2 (en) | 2006-04-21 | 2010-09-14 | Shell Oil Company | Non-ferromagnetic overburden casing |
US7610962B2 (en) | 2006-04-21 | 2009-11-03 | Shell Oil Company | Sour gas injection for use with in situ heat treatment |
US8083813B2 (en) | 2006-04-21 | 2011-12-27 | Shell Oil Company | Methods of producing transportation fuel |
US7683296B2 (en) | 2006-04-21 | 2010-03-23 | Shell Oil Company | Adjusting alloy compositions for selected properties in temperature limited heaters |
US7635023B2 (en) | 2006-04-21 | 2009-12-22 | Shell Oil Company | Time sequenced heating of multiple layers in a hydrocarbon containing formation |
US7604052B2 (en) | 2006-04-21 | 2009-10-20 | Shell Oil Company | Compositions produced using an in situ heat treatment process |
US7597147B2 (en) | 2006-04-21 | 2009-10-06 | Shell Oil Company | Temperature limited heaters using phase transformation of ferromagnetic material |
US8857506B2 (en) | 2006-04-21 | 2014-10-14 | Shell Oil Company | Alternate energy source usage methods for in situ heat treatment processes |
US7533719B2 (en) | 2006-04-21 | 2009-05-19 | Shell Oil Company | Wellhead with non-ferromagnetic materials |
US7673786B2 (en) | 2006-04-21 | 2010-03-09 | Shell Oil Company | Welding shield for coupling heaters |
US20070278344A1 (en) * | 2006-06-06 | 2007-12-06 | Pioneer Invention, Inc. D/B/A Pioneer Astronautics | Apparatus and Method for Producing Lift Gas and Uses Thereof |
US7871036B2 (en) | 2006-06-06 | 2011-01-18 | Pioneer Astronautics | Apparatus for generation and use of lift gas |
US7735777B2 (en) | 2006-06-06 | 2010-06-15 | Pioneer Astronautics | Apparatus for generation and use of lift gas |
US20100276141A1 (en) * | 2006-10-20 | 2010-11-04 | Shell Oil Company | Creating fluid injectivity in tar sands formations |
US7635024B2 (en) | 2006-10-20 | 2009-12-22 | Shell Oil Company | Heating tar sands formations to visbreaking temperatures |
US7631690B2 (en) | 2006-10-20 | 2009-12-15 | Shell Oil Company | Heating hydrocarbon containing formations in a spiral startup staged sequence |
US8555971B2 (en) | 2006-10-20 | 2013-10-15 | Shell Oil Company | Treating tar sands formations with dolomite |
US7562707B2 (en) | 2006-10-20 | 2009-07-21 | Shell Oil Company | Heating hydrocarbon containing formations in a line drive staged process |
US7845411B2 (en) | 2006-10-20 | 2010-12-07 | Shell Oil Company | In situ heat treatment process utilizing a closed loop heating system |
US7703513B2 (en) | 2006-10-20 | 2010-04-27 | Shell Oil Company | Wax barrier for use with in situ processes for treating formations |
US7677310B2 (en) | 2006-10-20 | 2010-03-16 | Shell Oil Company | Creating and maintaining a gas cap in tar sands formations |
US7677314B2 (en) | 2006-10-20 | 2010-03-16 | Shell Oil Company | Method of condensing vaporized water in situ to treat tar sands formations |
US7841401B2 (en) | 2006-10-20 | 2010-11-30 | Shell Oil Company | Gas injection to inhibit migration during an in situ heat treatment process |
US7673681B2 (en) | 2006-10-20 | 2010-03-09 | Shell Oil Company | Treating tar sands formations with karsted zones |
US7681647B2 (en) | 2006-10-20 | 2010-03-23 | Shell Oil Company | Method of producing drive fluid in situ in tar sands formations |
US7540324B2 (en) | 2006-10-20 | 2009-06-02 | Shell Oil Company | Heating hydrocarbon containing formations in a checkerboard pattern staged process |
US7717171B2 (en) | 2006-10-20 | 2010-05-18 | Shell Oil Company | Moving hydrocarbons through portions of tar sands formations with a fluid |
US7730946B2 (en) | 2006-10-20 | 2010-06-08 | Shell Oil Company | Treating tar sands formations with dolomite |
US7644765B2 (en) | 2006-10-20 | 2010-01-12 | Shell Oil Company | Heating tar sands formations while controlling pressure |
US8191630B2 (en) | 2006-10-20 | 2012-06-05 | Shell Oil Company | Creating fluid injectivity in tar sands formations |
US7730945B2 (en) | 2006-10-20 | 2010-06-08 | Shell Oil Company | Using geothermal energy to heat a portion of a formation for an in situ heat treatment process |
US7730947B2 (en) | 2006-10-20 | 2010-06-08 | Shell Oil Company | Creating fluid injectivity in tar sands formations |
US20100212893A1 (en) * | 2006-11-14 | 2010-08-26 | Behdad Moini Araghi | Catalytic down-hole upgrading of heavy oil and oil sand bitumens |
WO2008058400A1 (en) * | 2006-11-14 | 2008-05-22 | The University Of Calgary | Catalytic down-hole upgrading of heavy oil and oil sand bitumens |
US7841408B2 (en) | 2007-04-20 | 2010-11-30 | Shell Oil Company | In situ heat treatment from multiple layers of a tar sands formation |
US8662175B2 (en) | 2007-04-20 | 2014-03-04 | Shell Oil Company | Varying properties of in situ heat treatment of a tar sands formation based on assessed viscosities |
US7798220B2 (en) | 2007-04-20 | 2010-09-21 | Shell Oil Company | In situ heat treatment of a tar sands formation after drive process treatment |
US7832484B2 (en) | 2007-04-20 | 2010-11-16 | Shell Oil Company | Molten salt as a heat transfer fluid for heating a subsurface formation |
US7841425B2 (en) | 2007-04-20 | 2010-11-30 | Shell Oil Company | Drilling subsurface wellbores with cutting structures |
US7849922B2 (en) | 2007-04-20 | 2010-12-14 | Shell Oil Company | In situ recovery from residually heated sections in a hydrocarbon containing formation |
US8459359B2 (en) | 2007-04-20 | 2013-06-11 | Shell Oil Company | Treating nahcolite containing formations and saline zones |
US7931086B2 (en) | 2007-04-20 | 2011-04-26 | Shell Oil Company | Heating systems for heating subsurface formations |
US8381815B2 (en) | 2007-04-20 | 2013-02-26 | Shell Oil Company | Production from multiple zones of a tar sands formation |
US8327681B2 (en) | 2007-04-20 | 2012-12-11 | Shell Oil Company | Wellbore manufacturing processes for in situ heat treatment processes |
US8791396B2 (en) | 2007-04-20 | 2014-07-29 | Shell Oil Company | Floating insulated conductors for heating subsurface formations |
US8042610B2 (en) | 2007-04-20 | 2011-10-25 | Shell Oil Company | Parallel heater system for subsurface formations |
US7950453B2 (en) | 2007-04-20 | 2011-05-31 | Shell Oil Company | Downhole burner systems and methods for heating subsurface formations |
US9181780B2 (en) | 2007-04-20 | 2015-11-10 | Shell Oil Company | Controlling and assessing pressure conditions during treatment of tar sands formations |
US20080283249A1 (en) * | 2007-05-19 | 2008-11-20 | Zubrin Robert M | Apparatus, methods, and systems for extracting petroleum using a portable coal reformer |
US7654330B2 (en) | 2007-05-19 | 2010-02-02 | Pioneer Energy, Inc. | Apparatus, methods, and systems for extracting petroleum using a portable coal reformer |
US20080283247A1 (en) * | 2007-05-20 | 2008-11-20 | Zubrin Robert M | Portable and modular system for extracting petroleum and generating power |
US20100314136A1 (en) * | 2007-05-20 | 2010-12-16 | Zubrin Robert M | Systems and methods for generating in-situ carbon dioxide driver gas for use in enhanced oil recovery |
US9605523B2 (en) | 2007-05-20 | 2017-03-28 | Pioneer Energy, Inc. | Systems and methods for generating in-situ carbon dioxide driver gas for use in enhanced oil recovery |
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 |
US8011451B2 (en) | 2007-10-19 | 2011-09-06 | Shell Oil Company | Ranging methods for developing wellbores in subsurface formations |
US8196658B2 (en) | 2007-10-19 | 2012-06-12 | Shell Oil Company | Irregular spacing of heat sources for treating hydrocarbon containing formations |
US8272455B2 (en) | 2007-10-19 | 2012-09-25 | Shell Oil Company | Methods for forming wellbores in heated formations |
US8276661B2 (en) | 2007-10-19 | 2012-10-02 | Shell Oil Company | Heating subsurface formations by oxidizing fuel on a fuel carrier |
US8146661B2 (en) | 2007-10-19 | 2012-04-03 | Shell Oil Company | Cryogenic treatment of gas |
US8162059B2 (en) | 2007-10-19 | 2012-04-24 | Shell Oil Company | Induction heaters used to heat subsurface formations |
US8240774B2 (en) | 2007-10-19 | 2012-08-14 | Shell Oil Company | Solution mining and in situ treatment of nahcolite beds |
US7866388B2 (en) | 2007-10-19 | 2011-01-11 | Shell Oil Company | High temperature methods for forming oxidizer fuel |
US7866386B2 (en) | 2007-10-19 | 2011-01-11 | Shell Oil Company | In situ oxidation of subsurface formations |
US8113272B2 (en) | 2007-10-19 | 2012-02-14 | Shell Oil Company | Three-phase heaters with common overburden sections for heating subsurface formations |
US8536497B2 (en) | 2007-10-19 | 2013-09-17 | Shell Oil Company | Methods for forming long subsurface heaters |
US8146669B2 (en) | 2007-10-19 | 2012-04-03 | Shell Oil Company | Multi-step heater deployment in a subsurface formation |
US8172335B2 (en) | 2008-04-18 | 2012-05-08 | Shell Oil Company | Electrical current flow between tunnels for use in heating subsurface hydrocarbon containing formations |
US8177305B2 (en) | 2008-04-18 | 2012-05-15 | Shell Oil Company | Heater connections in mines and tunnels for use in treating subsurface hydrocarbon containing formations |
US8636323B2 (en) | 2008-04-18 | 2014-01-28 | Shell Oil Company | Mines and tunnels for use in treating subsurface hydrocarbon containing formations |
US8752904B2 (en) | 2008-04-18 | 2014-06-17 | Shell Oil Company | Heated fluid flow in mines and tunnels used in heating subsurface hydrocarbon containing formations |
US8562078B2 (en) | 2008-04-18 | 2013-10-22 | Shell Oil Company | Hydrocarbon production from mines and tunnels used in treating subsurface hydrocarbon containing formations |
US8162405B2 (en) | 2008-04-18 | 2012-04-24 | Shell Oil Company | Using tunnels for treating subsurface hydrocarbon containing formations |
US8151907B2 (en) | 2008-04-18 | 2012-04-10 | Shell Oil Company | Dual motor systems and non-rotating sensors for use in developing wellbores in subsurface formations |
US9528322B2 (en) | 2008-04-18 | 2016-12-27 | Shell Oil Company | Dual motor systems and non-rotating sensors for use in developing wellbores in subsurface formations |
US8691253B1 (en) * | 2008-05-28 | 2014-04-08 | Rhonda Tracy | Shark repellent |
US8450536B2 (en) | 2008-07-17 | 2013-05-28 | Pioneer Energy, Inc. | Methods of higher alcohol synthesis |
US8785699B2 (en) | 2008-07-17 | 2014-07-22 | Pioneer Energy, Inc. | Methods of higher alcohol synthesis |
US20100088951A1 (en) * | 2008-07-17 | 2010-04-15 | Pioneer Astronautics | Novel Methods of Higher Alcohol Synthesis |
US8261832B2 (en) | 2008-10-13 | 2012-09-11 | Shell Oil Company | Heating subsurface formations with fluids |
US8267170B2 (en) | 2008-10-13 | 2012-09-18 | Shell Oil Company | Offset barrier wells in subsurface formations |
US8220539B2 (en) | 2008-10-13 | 2012-07-17 | Shell Oil Company | Controlling hydrogen pressure in self-regulating nuclear reactors used to treat a subsurface formation |
US8256512B2 (en) | 2008-10-13 | 2012-09-04 | Shell Oil Company | Movable heaters for treating subsurface hydrocarbon containing formations |
US9129728B2 (en) | 2008-10-13 | 2015-09-08 | Shell Oil Company | Systems and methods of forming subsurface wellbores |
US9051829B2 (en) | 2008-10-13 | 2015-06-09 | Shell Oil Company | Perforated electrical conductors for treating subsurface formations |
US9022118B2 (en) | 2008-10-13 | 2015-05-05 | Shell Oil Company | Double insulated heaters for treating subsurface formations |
US8881806B2 (en) | 2008-10-13 | 2014-11-11 | Shell Oil Company | Systems and methods for treating a subsurface formation with electrical conductors |
US8353347B2 (en) | 2008-10-13 | 2013-01-15 | Shell Oil Company | Deployment of insulated conductors for treating subsurface formations |
US8267185B2 (en) | 2008-10-13 | 2012-09-18 | Shell Oil Company | Circulated heated transfer fluid systems used to treat a subsurface formation |
US8281861B2 (en) | 2008-10-13 | 2012-10-09 | Shell Oil Company | Circulated heated transfer fluid heating of subsurface hydrocarbon formations |
US8327932B2 (en) | 2009-04-10 | 2012-12-11 | Shell Oil Company | Recovering energy from a subsurface formation |
US8434555B2 (en) | 2009-04-10 | 2013-05-07 | Shell Oil Company | Irregular pattern treatment of a subsurface formation |
US8851170B2 (en) | 2009-04-10 | 2014-10-07 | Shell Oil Company | Heater assisted fluid treatment of a subsurface formation |
US8448707B2 (en) | 2009-04-10 | 2013-05-28 | Shell Oil Company | Non-conducting heater casings |
US20110203292A1 (en) * | 2009-09-23 | 2011-08-25 | Pioneer Energy Inc. | Methods for generating electricity from carbonaceous material with substantially no carbon dioxide emissions |
US8047007B2 (en) | 2009-09-23 | 2011-11-01 | Pioneer Energy Inc. | Methods for generating electricity from carbonaceous material with substantially no carbon dioxide emissions |
US9033042B2 (en) | 2010-04-09 | 2015-05-19 | Shell Oil Company | Forming bitumen barriers in subsurface hydrocarbon formations |
US9022109B2 (en) | 2010-04-09 | 2015-05-05 | Shell Oil Company | Leak detection in circulated fluid systems for heating subsurface formations |
US8701769B2 (en) | 2010-04-09 | 2014-04-22 | Shell Oil Company | Methods for treating hydrocarbon formations based on geology |
US9399905B2 (en) | 2010-04-09 | 2016-07-26 | Shell Oil Company | Leak detection in circulated fluid systems for heating subsurface formations |
US8701768B2 (en) | 2010-04-09 | 2014-04-22 | Shell Oil Company | Methods for treating hydrocarbon formations |
US9127523B2 (en) | 2010-04-09 | 2015-09-08 | Shell Oil Company | Barrier methods for use in subsurface hydrocarbon formations |
US8820406B2 (en) | 2010-04-09 | 2014-09-02 | Shell Oil Company | Electrodes for electrical current flow heating of subsurface formations with conductive material in wellbore |
US9127538B2 (en) | 2010-04-09 | 2015-09-08 | Shell Oil Company | Methodologies for treatment of hydrocarbon formations using staged pyrolyzation |
US8739874B2 (en) | 2010-04-09 | 2014-06-03 | Shell Oil Company | Methods for heating with slots in hydrocarbon formations |
US8631866B2 (en) | 2010-04-09 | 2014-01-21 | Shell Oil Company | Leak detection in circulated fluid systems for heating subsurface formations |
US8833453B2 (en) | 2010-04-09 | 2014-09-16 | Shell Oil Company | Electrodes for electrical current flow heating of subsurface formations with tapered copper thickness |
US9016370B2 (en) | 2011-04-08 | 2015-04-28 | Shell Oil Company | Partial solution mining of hydrocarbon containing layers prior to in situ heat treatment |
US9309755B2 (en) | 2011-10-07 | 2016-04-12 | Shell Oil Company | Thermal expansion accommodation for circulated fluid systems used to heat subsurface formations |
US20130161008A1 (en) * | 2011-12-22 | 2013-06-27 | Argonne National Laboratory | Preparation and use of nano-catalysts for in-situ reaction with kerogen |
US9181467B2 (en) * | 2011-12-22 | 2015-11-10 | Uchicago Argonne, Llc | Preparation and use of nano-catalysts for in-situ reaction with kerogen |
US10047594B2 (en) | 2012-01-23 | 2018-08-14 | Genie Ip B.V. | Heater pattern for in situ thermal processing of a subsurface hydrocarbon containing formation |
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