Nothing Special   »   [go: up one dir, main page]

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 PDF

Info

Publication number
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
Authority
US
United States
Prior art keywords
oil
reservoir
hydrogen
situ
catalyst
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired - Lifetime
Application number
US717256A
Inventor
William P Banks
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Jersey Production Research Co
Original Assignee
Jersey Production Research Co
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Jersey Production Research Co filed Critical Jersey Production Research Co
Priority to US717256A priority Critical patent/US3051235A/en
Application granted granted Critical
Publication of US3051235A publication Critical patent/US3051235A/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Images

Classifications

    • EFIXED CONSTRUCTIONS
    • E21EARTH OR ROCK DRILLING; MINING
    • E21BEARTH OR ROCK DRILLING; OBTAINING OIL, GAS, WATER, SOLUBLE OR MELTABLE MATERIALS OR A SLURRY OF MINERALS FROM WELLS
    • E21B43/00Methods or apparatus for obtaining oil, gas, water, soluble or meltable materials or a slurry of minerals from wells
    • E21B43/16Enhanced recovery methods for obtaining hydrocarbons
    • E21B43/24Enhanced recovery methods for obtaining hydrocarbons using heat, e.g. steam injection
    • E21B43/243Combustion 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.

Landscapes

  • 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
US717256A 1958-02-24 1958-02-24 Recovery of petroleum crude oil, by in situ combustion and in situ hydrogenation Expired - Lifetime US3051235A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
US717256A US3051235A (en) 1958-02-24 1958-02-24 Recovery of petroleum crude oil, by in situ combustion and in situ hydrogenation

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US717256A US3051235A (en) 1958-02-24 1958-02-24 Recovery of petroleum crude oil, by in situ combustion and in situ hydrogenation

Publications (1)

Publication Number Publication Date
US3051235A true US3051235A (en) 1962-08-28

Family

ID=24881309

Family Applications (1)

Application Number Title Priority Date Filing Date
US717256A Expired - Lifetime US3051235A (en) 1958-02-24 1958-02-24 Recovery of petroleum crude oil, by in situ combustion and in situ hydrogenation

Country Status (1)

Country Link
US (1) US3051235A (en)

Cited By (51)

* Cited by examiner, † Cited by third party
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
WO2004097159A2 (en) * 2003-04-24 2004-11-11 Shell Internationale Research Maatschappij B.V. Thermal processes for subsurface formations
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
WO2008058400A1 (en) * 2006-11-14 2008-05-22 The University Of Calgary Catalytic down-hole upgrading of heavy oil and oil sand bitumens
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
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
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)

* Cited by examiner, † Cited by third party
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

Patent Citations (8)

* Cited by examiner, † Cited by third party
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)

* Cited by examiner, † Cited by third party
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
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
US5054551A (en) * 1990-08-03 1991-10-08 Chevron Research And Technology Company In-situ heated annulus refining process
US5145003A (en) * 1990-08-03 1992-09-08 Chevron Research And Technology Company Method for 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
US6328104B1 (en) 1998-06-24 2001-12-11 World Energy Systems Incorporated Upgrading and recovery of heavy crude oils and natural bitumens 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
US20110088904A1 (en) * 2000-04-24 2011-04-21 De Rouffignac Eric Pierre In situ recovery from a hydrocarbon containing formation
US8225866B2 (en) 2000-04-24 2012-07-24 Shell Oil Company In situ recovery from a hydrocarbon containing formation
US8789586B2 (en) 2000-04-24 2014-07-29 Shell Oil Company In situ recovery from a hydrocarbon containing formation
US7798221B2 (en) 2000-04-24 2010-09-21 Shell Oil Company In situ recovery from a hydrocarbon containing formation
US8485252B2 (en) 2000-04-24 2013-07-16 Shell Oil Company In situ recovery from a hydrocarbon containing formation
US8608249B2 (en) 2001-04-24 2013-12-17 Shell Oil Company In situ thermal processing of an oil shale formation
US7735935B2 (en) 2001-04-24 2010-06-15 Shell Oil Company In situ thermal processing of an oil shale formation containing carbonate minerals
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
US8627887B2 (en) 2001-10-24 2014-01-14 Shell Oil Company In situ recovery from a hydrocarbon containing formation
US7461691B2 (en) 2001-10-24 2008-12-09 Shell Oil Company In situ recovery from a hydrocarbon containing formation
US7219734B2 (en) 2002-10-24 2007-05-22 Shell Oil Company Inhibiting wellbore deformation during in situ thermal processing of a hydrocarbon containing formation
US8200072B2 (en) 2002-10-24 2012-06-12 Shell Oil Company Temperature limited heaters for heating subsurface formations or wellbores
US20040140096A1 (en) * 2002-10-24 2004-07-22 Sandberg Chester Ledlie Insulated conductor temperature limited heaters
US8224164B2 (en) 2002-10-24 2012-07-17 Shell Oil Company Insulated conductor temperature limited heaters
US8224163B2 (en) 2002-10-24 2012-07-17 Shell Oil Company Variable frequency temperature limited heaters
US7360588B2 (en) 2003-04-24 2008-04-22 Shell Oil Company Thermal processes for subsurface formations
US20090071647A1 (en) * 2003-04-24 2009-03-19 Vinegar Harold J Thermal processes for subsurface formations
WO2004097159A2 (en) * 2003-04-24 2004-11-11 Shell Internationale Research Maatschappij B.V. Thermal processes for subsurface formations
US8579031B2 (en) 2003-04-24 2013-11-12 Shell Oil Company Thermal processes for subsurface formations
US7640980B2 (en) 2003-04-24 2010-01-05 Shell Oil Company Thermal processes for subsurface formations
WO2004097159A3 (en) * 2003-04-24 2006-05-18 Shell Int Research Thermal processes for subsurface formations
US7942203B2 (en) 2003-04-24 2011-05-17 Shell Oil Company Thermal processes for subsurface formations
US20070131411A1 (en) * 2003-04-24 2007-06-14 Vinegar Harold J Thermal processes for subsurface formations
US20050269090A1 (en) * 2004-04-23 2005-12-08 Vinegar Harold J Temperature limited heaters with thermally conductive fluid used to heat subsurface formations
US7431076B2 (en) 2004-04-23 2008-10-07 Shell Oil Company Temperature limited heaters using modulated DC power
US7481274B2 (en) 2004-04-23 2009-01-27 Shell Oil Company Temperature limited heaters with relatively constant current
US7490665B2 (en) 2004-04-23 2009-02-17 Shell Oil Company Variable frequency temperature limited heaters
US7370704B2 (en) 2004-04-23 2008-05-13 Shell Oil Company Triaxial temperature limited heater
US7353872B2 (en) 2004-04-23 2008-04-08 Shell Oil Company Start-up of temperature limited heaters using direct current (DC)
US20050269093A1 (en) * 2004-04-23 2005-12-08 Sandberg Chester L Variable frequency temperature limited heaters
US20050269092A1 (en) * 2004-04-23 2005-12-08 Vinegar Harold J Vacuum pumping of conductor-in-conduit heaters
US20050269089A1 (en) * 2004-04-23 2005-12-08 Sandberg Chester L Temperature limited heaters using modulated DC power
US20050269088A1 (en) * 2004-04-23 2005-12-08 Vinegar Harold J Inhibiting effects of sloughing in wellbores
US20050269094A1 (en) * 2004-04-23 2005-12-08 Harris Christopher K Triaxial temperature limited heater
US7357180B2 (en) 2004-04-23 2008-04-15 Shell Oil Company Inhibiting effects of sloughing in wellbores
US7383877B2 (en) 2004-04-23 2008-06-10 Shell Oil Company Temperature limited heaters with thermally conductive fluid used to heat subsurface formations
US8355623B2 (en) 2004-04-23 2013-01-15 Shell Oil Company Temperature limited heaters with high power factors
US7986869B2 (en) 2005-04-22 2011-07-26 Shell Oil Company Varying properties along lengths of temperature limited heaters
US7942197B2 (en) 2005-04-22 2011-05-17 Shell Oil Company Methods and systems for producing fluid from an in situ conversion process
US8230927B2 (en) 2005-04-22 2012-07-31 Shell Oil Company Methods and systems for producing fluid from an in situ conversion process
US7575052B2 (en) 2005-04-22 2009-08-18 Shell Oil Company In situ conversion process utilizing a closed loop heating system
US7575053B2 (en) 2005-04-22 2009-08-18 Shell Oil Company Low temperature monitoring system for subsurface barriers
US7860377B2 (en) 2005-04-22 2010-12-28 Shell Oil Company Subsurface connection methods for subsurface heaters
US7435037B2 (en) 2005-04-22 2008-10-14 Shell Oil Company Low temperature barriers with heat interceptor wells for in situ processes
US8233782B2 (en) 2005-04-22 2012-07-31 Shell Oil Company Grouped exposed metal heaters
US8224165B2 (en) 2005-04-22 2012-07-17 Shell Oil Company Temperature limited heater utilizing non-ferromagnetic conductor
US7831134B2 (en) 2005-04-22 2010-11-09 Shell Oil Company Grouped exposed metal heaters
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
US7546873B2 (en) 2005-04-22 2009-06-16 Shell Oil Company Low temperature barriers for use with in situ processes
US8070840B2 (en) 2005-04-22 2011-12-06 Shell Oil Company Treatment of gas from an in situ conversion process
US20070137857A1 (en) * 2005-04-22 2007-06-21 Vinegar Harold J Low temperature monitoring system for subsurface barriers
US7527094B2 (en) 2005-04-22 2009-05-05 Shell Oil Company Double barrier system for an in situ conversion process
US7500528B2 (en) 2005-04-22 2009-03-10 Shell Oil Company Low temperature barrier wellbores formed using water flushing
US7584789B2 (en) 2005-10-24 2009-09-08 Shell Oil Company Methods of cracking a crude product to produce additional crude products
US7559367B2 (en) 2005-10-24 2009-07-14 Shell Oil Company Temperature limited heater with a conduit substantially electrically isolated from the formation
US7591310B2 (en) 2005-10-24 2009-09-22 Shell Oil Company Methods of hydrotreating a liquid stream to remove clogging compounds
US7549470B2 (en) 2005-10-24 2009-06-23 Shell Oil Company Solution mining and heating by oxidation for treating hydrocarbon containing formations
US7635025B2 (en) 2005-10-24 2009-12-22 Shell Oil Company Cogeneration systems and processes for treating hydrocarbon containing formations
US7556096B2 (en) 2005-10-24 2009-07-07 Shell Oil Company Varying heating in dawsonite zones in hydrocarbon containing formations
US7556095B2 (en) 2005-10-24 2009-07-07 Shell Oil Company Solution mining dawsonite from hydrocarbon containing formations with a chelating agent
US8606091B2 (en) 2005-10-24 2013-12-10 Shell Oil Company Subsurface heaters with low sulfidation rates
US7559368B2 (en) 2005-10-24 2009-07-14 Shell Oil Company Solution mining systems and methods for treating hydrocarbon containing formations
US7562706B2 (en) 2005-10-24 2009-07-21 Shell Oil Company Systems and methods for producing hydrocarbons from tar sands formations
US7581589B2 (en) 2005-10-24 2009-09-01 Shell Oil Company Methods of producing alkylated hydrocarbons from an in situ heat treatment process liquid
US8151880B2 (en) 2005-10-24 2012-04-10 Shell Oil Company Methods of making transportation fuel
US9605522B2 (en) 2006-03-29 2017-03-28 Pioneer Energy, Inc. Apparatus and method for extracting petroleum from underground sites using reformed gases
US20090236093A1 (en) * 2006-03-29 2009-09-24 Pioneer Energy, Inc. Apparatus and Method for Extracting Petroleum from Underground Sites Using Reformed Gases
US8602095B2 (en) 2006-03-29 2013-12-10 Pioneer Energy, Inc. Apparatus and method for extracting petroleum from underground sites using reformed gases
US7912358B2 (en) 2006-04-21 2011-03-22 Shell Oil Company Alternate energy source usage for in situ heat treatment processes
US20100272595A1 (en) * 2006-04-21 2010-10-28 Shell Oil Company High strength alloys
US7631689B2 (en) 2006-04-21 2009-12-15 Shell Oil Company Sulfur barrier for use with in situ processes for treating formations
US7866385B2 (en) 2006-04-21 2011-01-11 Shell Oil Company Power systems utilizing the heat of produced formation fluid
US8192682B2 (en) 2006-04-21 2012-06-05 Shell Oil Company High strength alloys
US7785427B2 (en) 2006-04-21 2010-08-31 Shell Oil Company High strength alloys
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

Similar Documents

Publication Publication Date Title
US3051235A (en) Recovery of petroleum crude oil, by in situ combustion and in situ hydrogenation
US5145003A (en) Method for in-situ heated annulus refining process
US3170517A (en) Fracturing formation and stimulation of wells
US4296969A (en) Thermal recovery of viscous hydrocarbons using arrays of radially spaced horizontal wells
US3120264A (en) Recovery of oil by in situ combustion
US3434541A (en) In situ combustion process
US4116275A (en) Recovery of hydrocarbons by in situ thermal extraction
US2897894A (en) Recovery of oil from subterranean reservoirs
US5273111A (en) Laterally and vertically staggered horizontal well hydrocarbon recovery method
US2946382A (en) Process for recovering hydrocarbons from underground formations
US3692111A (en) Stair-step thermal recovery of oil
US2910123A (en) Method of recovering petroleum
US3997004A (en) Method for recovering viscous petroleum
US4127172A (en) Viscous oil recovery method
US4387770A (en) Process for selective injection into a subterranean formation
US3003555A (en) Oil production from unconsolidated formations
US3913671A (en) Recovery of petroleum from viscous petroleum containing formations including tar sand deposits
US3272261A (en) Process for recovery of oil
US3361201A (en) Method for recovery of petroleum by fluid injection
US3167121A (en) Method for producing high viscosity oil
US3246693A (en) Secondary recovery of viscous crude oil
US3349849A (en) Thermoaugmentation of oil production from subterranean reservoirs
US4566537A (en) Heavy oil recovery
US4961467A (en) Enhanced oil recovery for oil reservoir underlain by water
US3024841A (en) Method of oil recovery by in situ combustion