US3110345A - Low temperature reverse combustion process - Google Patents

Low temperature reverse combustion process Download PDF

Info

Publication number
US3110345A
US3110345A US795636A US79563659A US3110345A US 3110345 A US3110345 A US 3110345A US 795636 A US795636 A US 795636A US 79563659 A US79563659 A US 79563659A US 3110345 A US3110345 A US 3110345A
Authority
US
United States
Prior art keywords
oil
combustion
formation
air
well
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
US795636A
Inventor
Denzel W Reed
Ronald L Reed
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.)
Gulf Research and Development Co
Original Assignee
Gulf Research and Development 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 Gulf Research and Development Co filed Critical Gulf Research and Development Co
Priority to US795636A priority Critical patent/US3110345A/en
Application granted granted Critical
Publication of US3110345A publication Critical patent/US3110345A/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
    • E21B43/2401Enhanced recovery methods for obtaining hydrocarbons using heat, e.g. steam injection by means of electricity
    • 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 invention relates to the production of oil by insitu combustion in an oil-bearing formation and more particularly to an improved reverse combustion process.
  • oxygen-containing gas is injected into the oil-bearing formation at one well, called the injection well, and oil in the formation is ignited at that well.
  • the injection of the oxygen-containing gas is continued to force oil in the formation to an adjacent well, called the production well, through which the oil is lifted to the surface.
  • the production well which is ordinarily called a forward burning process, the movement of the combustion front and the flow of the oxygen-containing gas and products of combustion are toward the production well.
  • the forward burning in-situ combustion process has several very desirable characteristics. Once the combustion has started, the products of combustion traveling ahead of the combustion front distill lighter fractions from the oil and leave only the very heavy ends in the form of coke to be burned as the combustion front moves outward from the injection well. The portion of the formation behind the combustion front is clean and completely stripped of hydrocarbons. Thus, the forward burning process results in a minimum consumption of the oil in the formation.
  • the oil ahead of the combustion front may be a heavy, highly viscous oil.
  • the oil and formation ahead of the cornbustion front are relatively cold. Hence, the viscosity of the oil remains high.
  • Ahead of the combustion front is a multi-phase mixture which may include liquid and gaseous hydrocarbons, gaseous products of combustion, and condensed water.
  • the water may be connate water originally present in the formation, water resulting from condensation of combustion products, or both.
  • the presence of the several fluid phases in the formation greatly reduces the permeability of the formation to any one phase. As a result of these factors, often the resistance to flow is so high it is not possible to inject an oxygen-containing gas into a formation at rates high enough to allow economic production by a forward burning process or, in some instances, to maintain combustion.
  • An in-situ combustion method that has been developed for the production of heavy oils from formations such as tar sands is the reverse combustion process.
  • an ox gen-containing gas is injected into the formation at the injection well and oil in the formation is ignited at an adjacent production well.
  • the combustion front then moves from the production well towards the injection well.
  • the oil produced by the process and the combustion products move in a direction opposite that of the combustion front and are discharged from the formation into the production well.
  • the reverse com- 3 .11345 Patented Nov. 12, 1%53 bustion process the oil that is moved through the formation is hot and moves through a hot formation of increased permeability.
  • the conventional reverse combustion process has an important disadvantage in that only a portion of the oil in the formation is burned or produced. The remainder of the oil is coked in place in the formation and is left in the formation as the combustion front moves to wards the injection well. The coke represents oil that cannot be recovered from the formation. The injection of additional air into the formation after the combustion front has moved to the injection well merely burns the coke in place and produces carbon monoxide, carbon dioxide, and water.
  • this disadvantage of the reverse combustion process in many oil-bearing formations of low permeability or containing heavy oils, or in some partially depleted formations, it is the only effective method of recovering oil from the pay zone.
  • This invention resides in a low temperature reverse combustion process in which oil in a fluid form remains in the pay zone after the combustion front has passed and that oil may then be recovered from the hot formation by an appropriate subsequent secondary recovery step.
  • Reverse combustion of the low temperature type is maintained and the peak temperature is controlled within narrow limits by regulation of the flux of the oxygen-containing gas injected into the formation.
  • the term flux refers to the rate of injection of the gas in terms of volume of gas injected per unit area of the combustion front per unit of time.
  • FIGURE 1 is a diagrammatic illustration of experimental apparatus set up to observe the in-situ combustion process of this invention.
  • FIGURE 2 is a diagrammatic sectional view of a well adapted to perform a low temperature reverse combustion process according to one embodiment of this invention.
  • FIGURE 3 is a graph in which the peak temperatures attained by tar sands during experimental runs are plotted against the air flux.
  • FIGURE 4 is a graph in which the percent of oil in the tar sand that was recovered by several experimental runs of in-situ combustion processes is plotted against the air flux.
  • FIGURE 5 is a graph in which the st-andmd cubic feet of air injected to recover a barrel of oil is plotted against air flux for several experimental runs.
  • the important advantage in the process of this invention resides in leaving a liquid residue in the oil-bearing formation after the reverse combustion step has been completed.
  • the liquid residue being hot and in a hot formation can then be recovered by additional steps, for example, a forward combustion step, a gas repressuring operation, a water flood operation, or a fracture-gravity drainage step.
  • additional steps for example, a forward combustion step, a gas repressuring operation, a water flood operation, or a fracture-gravity drainage step.
  • the combination of low temperature reverse combustion with one of these additional recovery steps frequently gives rise to an improved process, with an improved oil recovery and improved over-ail economics.
  • the combination of low temperature reverse combustion with forward combustion as a addition to the oil.
  • the residue in the formation following the reverse combustion step is liquid depends upon the amount and extent of :coldng of the oil 1 it in the formation.
  • the extent of coking in turn will depend on the temperature reached by the formation as the combustion front passes through it and the nature of the oil left in the formation.
  • FIG. 1 of the drawings a compressed air container 1% is provided with a discharge line 32 in which there is a reducing valve 14 to control the pressure.
  • a metering device v15, illustrated as a rotameter, in line 12 allows continuous measurement for control or" the rate of llow of the air.
  • a line 18 connects the discharge end of the rotameter 16 with the inlet of a combustion tube indicated generally by reference numeral 22 through a pressure reducing valve 23-.
  • Combustion tube 22 illustrated in FZGURE 1 consists of a -central tube 24 closed at its upper end except for connection with line 1'8 and at its lower end except for connection with a discharge line 25.
  • Tube 24- is surrounded with a thin layer of insulation 28 around which are assembled electrical heaters 36 supplied with electrical power leads 32.
  • thermocouple 34 is positioned in the center of the combustion tube 2 by passing it through a thermocouple well 36 and a gas tight seal 38 located on the end of the thermocouple well 36.
  • a thermocouple 4% is located with its junction on insulation 28 by passing it through a hole 42 in heater 30.
  • An outer layer of insulation 44 encloses the complete combustion tube assembly 22.
  • Thermocouples 34 and 4t and power leads 32 are connected to a control system (not shown in FIGURE 1) in such a way that whenever thermocouple 34 is hotter than thermocouple 4% electrical current is supplied to V heater 3%, and whenever thermocouple 413 is hotter than thermocouple 34 electrical curernt is not supplied to heater 3% Furthermore, the controller is so designed that the rate of heat generated by the heater 3% is in proportion to the rate at which the temperature at the center of the tube is increasing. Controllers of this kind are well known to those versed in the art. For the purpose of maintaining the entire combustion tube 22 in a locally adiabatic condition, a series of individual heaters 3t each with its associated thermocouple pairs (34 and 46'), power leads 32, and proportional controllers, are provided along the length of the tube.
  • Discharge line 26 opens into the upper end of a separator 46.
  • An outlet line 4% provided with a valve 5% allows 4 withdrawal or" liquid collected in the separator as.
  • Gaseous products and entrained liquids from the separator as are delivered through a line 5'2 to the upper end of a condenser coil 5%.
  • the mixture of gas and liquid products from the condenser coil 54- is delivered through line 58 to a separator 60.
  • Liquid products collected in separator 6%- are discharged through a line 62. provided with a valve 64.
  • Uncondensed gaseous products from separator together with entrained liquids pass through a side outlet line 66 into the bottom of a high voltage electrical preoipitator as where entrained liquids are removed from the gases and drain through a discharge line 7% into a receiver '72.
  • Liquid products collected in receiver 72 are discharged through a line 74 provided with a valve '75.
  • Gaseous products are discharged from the top of the electrical precipitator through a line 78 into a gas meter 39 which measures the how rate of non-co-nde-nsible gaseous products from precipitator 6-8. Gaseous products from the gas meter 8% are discharged to the atmosphere through line 82.
  • thermocouple wells 36 In preparation for each of the experimental runs, suitably sized rods were insented through thermocouple wells 36 flush with the inside wall of the combustion tube 24 and one end plate was bolted in position to close one end of the tube. Heating'elements 36 were turned on and the entire tube heated to about 200 F. Tar sand was preheated to 200 F. and carefully tamped in place until the tube 24- was full. The other end plate was bolted in position and the rods in the thermocouple wells were driven into the center of the sand and then removed. Thermocouples 34 were inserted through the thermocouple wells 38 and into the center of the sand thus occupying the space created by removal of the rods. The complete assembly 22 was then allowed to cool to room temperature.
  • an electric flange heater 84 is heated as rapidly as possible to a temperature sufiiciently high to initiate combustion at the air flux used.
  • air is admitted to the tube 24 through the line 18 at the do sired rate.
  • a combustion zone is formed and moves from the bottom to the top of the tube.
  • the plot of the percent of oil recovered against the air flux in FIGURE 4 shows the advantages of this invention in causing increased recovery of oil.
  • the dotted line to the left of the intersection of the lines in FIG- URE 4 indicates the total recovery of oil and the solid line to the left of the intersection indicates the recovery during the low temperature reverse combustion step.
  • additional oil was recovered upon injection of air after reverse combustion had ceased.
  • the recovery was increased from 17% to 59% of the oil in the tar sand.
  • no additional oil was recovered after the reverse combustion had proceeded from the outlet to the inlet end of the combustion tubing.
  • FIG- URE 5 Another advantage of this invention is shown in FIG- URE 5, where the ratio of air injected to oil recovered is plotted against the air flux.
  • the dotted line to the left of the intersection of the lines in FIGURE 5 indicates the over-all air-oil ratio for a process consisting of low temperature reverse combustion followed by a forward combustion step.
  • the solid line to the left of the intersection of the lines in FIGURE 5 indicates the air-oil ratio during the low temperature reverse combustion step.
  • the curve in FIGURE 3 shows the relation between the peak temperature attained and the air flux at substantially atmospheric pressure. Higher pressures result in lower peak temperatures for a given air flux. For example, an air flux of 55 standard cubic feet per square foot per :hour passed through a tar sand under a pressure of 450 pounds per square inch, resulted in 'a peak temperature of 550 F. At atmospheric pressure the same air flux would result in a temperature of approximately 855 F. However, an air flux less than 40 standard cubic feet per square foot per hour in a reverse combustion 6 process would allow recovery of additional oil from the formation after the reverse combustion process is completed in a reverse combustion process performed at high pressures as well as low pressures because of the lower peak temperatures reached.
  • FIGURE 2 of the drawings One well structure adapted for carrying out the process of this invention is illustrated in FIGURE 2 of the drawings.
  • a well indicated generally by reference numeral is drilled through an oil-bearing formation 92 between a cap rock 94 and an underlying base rock 96 to a total depth 98.
  • Casing 1% is run into the well and cemented in place by a sheath 1492 of cement in accordance with the usual techniques for thermal recovery processes.
  • the casing 160 and cement sheath 102 are perforated at 104 near the upper limits of the pay zone 92 and at 106 near the bottom of the pay Zone.
  • a large substantially horizontal radial fracture 108 is made in the lower portion of the pay Zone.
  • a similar fracture 114 is made near the upper limit of the pay zone.
  • a packer 112 is run into the casing 1% and set at a position between the upper perforations 104 and lower perforations i496.
  • Tubing 114 extends from the well head through packer 112 and opens at its lower end within the casing adjacent the perforations 106.
  • Tubing 114 extends upwardly through a cap 116 closing the upper end of the well and is connected with a line 118 for delivery of oil produced from the well.
  • An air supply line 129 extends through the cap 116 and communicates with the annular space 122 between the casing 10% and the tubing 114.
  • a suitable burner is positioned in the well adjacent the perforations 1%.
  • a mixture of a fuel and air is burned adjacent the perforations 1G6 and the products of combustion forced into the fracture 11% to heat the formation around fracture 108 to a temperature high enough to initiate reverse combustion.
  • Air is introduced into the well through line and discharged through perforations 164 into fracture 110. The air flows downwardly through the pay zone 92 to cause in-situ combustion of oil to begin in the hot formation adjacent the fracture 1&8.
  • the combustion front moves upwardly countercurrent to the flow of air, and oil produced from the formation is removed through line 114. injection of air is continued at a rate controlled to maintain the temperature in the formation below 750 F.
  • the substantially linear flow from the upper fracture to the lower fracture facilitates control of the air flux.
  • the combustion front reaches the upper fracture 110
  • the flow of air can be stopped and production of the hot oil remaining in the formation obtained by a gas repressuring process, a water injection process, or by gravity drainage. It is preferred, however, to follow the low temperature reverse combustion step by a forward combustion process by injection of additional air, thus effectively removing substantially all of the remaining oil from the heated pay zone.
  • Any gravity drainage that may occur in the pay zone favors increased recovery of the oil when the production is delivered into the lower fracture during both the low temperature reverse combustion and subsequent recovery steps.
  • the fractures through which air is injected and the production recovered can be reversed, but the advantage of gravity drainage is not obtained if the direction of flow is reversed.
  • Ignition of oil in the formation is accomplished by heating the formation to a temperature sufficiently high that when contacted with an oxygen-containing gas ignition will occur.
  • a preferred method is to inject air into the formation at the injection well until it can be produced at the production Well with an oxygen content high enough to cause ignition of oil in the formation when the formation is heated. Air injection is then stopped and a gas burner ignited in the production well. The products of combustion are displaced into the formation until the formation is heated-for a radial distance of at least a few inches from the borehole of the production well to a temperature higher than the peak temperature attained in a low temperature reverse combustion process at the air fiux existing in the heated zone when air injection is resumed. The burner is then removed from the production well and air again injected into the formation at the injection well. Ignition occurs as air reaches the heated zone in the formation.
  • the formation surrounding the production well is heated by conduction or by gases passed over the heater and into the formation. If air is passed over the electric heater, forward combustion may be initiated at the production well. Forward combustion can be continued until an injection pressure approaching the overburden pressure on the formation is attained. The injection of air at the production well is then stopped and air is injected at the injection well. When the air from the injection well reaches the zone of forward combustion, the combustion is converted to reverse combustion. After reverse combustion has started, the air flux is adjusted to cause the desired flow temperature reverse combustion.
  • the process of this invention can be used in other well arrangements.
  • one well may be used as an input well and an adjacent well as a production well.
  • Another arrangement that can be used effectively is to use wells in one row as injection wells and in an adjacent row as production wells.
  • the location at which oil is delivered from the formation in channels for delivery to the well head and recovery is generally referred to as the production wellin the description of this invention.
  • the invention is not limited to a process using separate injection and production wells and that the term production well includes within its scope any production zone spaced from the injection zone through which oil is produced from the formation into channels suitable for delivery of the oil, gas, and combustion products to the well head.
  • a well is drilled to a total depth of 575 feet through a pay zone in the interval of 530 to 565 feet.
  • Casing is run into the well to total depth and cemented by conventional practice.
  • the casing and surrounding cement sheath are then severed by a ring shaped charge at a depth of 560 feet and again at a depth of 535 feet.
  • a packer is set in the casing between the two levels at which the casing is cut.
  • the formation is then fractured through the lower opening in the casing to form a horizontal fracture having an estimated radius of 100 feet, and the fracture is propped open with coarse sand. With the packer in place but closed to isolate the lower fracture, a horizontal fracture having an estimated radius of 100 feet is formed through the opening in the casing at a depth of 535 feet.
  • the upper fracture is also propped open with coarse sand.
  • a burner is run through the packer to a position adjacent the lower fracture and a combustible mixture of lease gas and air delivered to the burner at a rate of 2000 cubic feet of lease gas per hour and burned below the packer.
  • the hot products of combustion are displaced from the borehole into the lower fracture to heat the formation adjacent the fracture to a temperature estimated to range between 1060" F. and 750 F.
  • the burner is pulled from the hole and tubing run through j the packer to a position with its lower end opening adja- 'ly to the upper fracture.
  • Air is then displaced into the upper fracture at a rate of 600,609 standard cubic feet per hour causin an air flux of approximately 20 standard cubic feet per square foot per hour at the combustion front between the upper and lower fracture.
  • low temperature reverse combustion of the oil in the formation is initiated.
  • the injection of air is continued to cause the combustion front'to move upward-
  • a mixture of hot oil, gas, and combustion products is delivered through the bottom fracture into the borehole and lifted through the tubing to the well head.
  • the process of this invention results in the production of an oil of relatively low specific gravity.
  • the production of low specific gravity oil during the low temperature reverse combustion process is believed to be attributable to an fractionation of light ends out of the oil by the advancing thermal wave in conjunction with the predominantly inert gas atmosphereprovided by the nitrogen content of injected air together with products of combustion which are accumulating in concentration the temperature increases.
  • the oil produced in the low temperature reverse combustion is frequently clear and amber in color rather than the dark oil produced in the reverse combustion processes of the prior art.
  • low temperature reverse combustion is used to designate a reverse combustion process in which the peak temperature is low enough that fluid oil remains in the formation after completion of the reverse combustion process. That fluid oil is hot and can then be recovered from the hot formation in a subsequent recovery step and thereby increase the amount of oil recovered from the formation.
  • An in-situ combustion process for the recovery of oil from an oil-bearing subsurface formation penetrated by an injection well and a production well spaced from the injection well comprising displam'ng air down the injection well into the oil-bearing formation and through the oil-bearing formation to the production well, heating oil in the oil-bearing formation adjacent the production well to a temperature whereby said oil ignites upon contact with the air displaced through the formation, continuing the displacement of air into the formation at a rate controlled to give an air flux at the combustion front less than about 40 std. cut. ft./sq. ft./hr. to cause reverse combustion to proceed at a temperature below approximately 750 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)

Description

N 1963 D. w. REED ETAL LOW TEMPERATURE REVERSE COMBUSTION PROCESS 3 Sheets-Sheet 1 Filed Feb. 26, 1959 Lap,
Y 5 w mp0 2 mi. N W W y L0 2 MM a; Y B
Nov. 12, 1963 11w. REED ETAL 3,110,345
LOW TEMPERATURE REVERSE COMBUSTION PROCESS Filed Feb. 26, 1959 3 Sheets-Sheet 2 /o & 900 o y k t 800 /o & /6) g 700 k 500 9 x R Y q, 500 v m R: 400 W 0 2o 40 60 a0 ma .4/ FLUX $0 6. .fzf. INVENTORS /(-Ks? oz-wzsz (A9660 P15. 5 B 90N440 4. 4560 ATTORNEY Nov. 12, 1963 D. w. REED ETAL 3,110,345
LOW TEMPERATURE REVERSE COMBUSTION PROCESS Filed Feb. 26, 1959 a Sheets-Sheet s 0 20 40 60 a0 /00 4/? 520x, sO /(AAXE 5:) x 0 1 15.4 3 40,000 \I a 50,000 E 2 Q q 20,000 Q L 4/5 540x, sax-705% r!) P 5 INVENTORS 5' 05/vz54 1445550 ea/v4.40 1.2550 BY ATTORNEY ite tree 3,11%,345 LOW TEMPERATURE REVERSE CGIWEBUSTEGN PRGQEES Benz-21W. Reed, Pittsburgh, and Ronald L. Reed, Allison Park, Pa, assignors to Gulf Research 8; Development ilompany, *rittsbnrgh, Pan, a corporation of Delaware Filed Feb. 26, 1959, Ser. No. 795,536 ll Claim. (Cl. tee-11 This invention relates to the production of oil by insitu combustion in an oil-bearing formation and more particularly to an improved reverse combustion process.
In the conventional in-situ combustion process, an
oxygen-containing gas is injected into the oil-bearing formation at one well, called the injection well, and oil in the formation is ignited at that well. The injection of the oxygen-containing gas is continued to force oil in the formation to an adjacent well, called the production well, through which the oil is lifted to the surface. In that process, which is ordinarily called a forward burning process, the movement of the combustion front and the flow of the oxygen-containing gas and products of combustion are toward the production well.
The forward burning in-situ combustion process has several very desirable characteristics. Once the combustion has started, the products of combustion traveling ahead of the combustion front distill lighter fractions from the oil and leave only the very heavy ends in the form of coke to be burned as the combustion front moves outward from the injection well. The portion of the formation behind the combustion front is clean and completely stripped of hydrocarbons. Thus, the forward burning process results in a minimum consumption of the oil in the formation.
Several factors often encountered in formations in which production by in-situ combustion may be desirable prevent the effective use of a forward burning process. The oil ahead of the combustion front may be a heavy, highly viscous oil. During the major part of the forward burning process, the oil and formation ahead of the cornbustion front are relatively cold. Hence, the viscosity of the oil remains high. Ahead of the combustion front is a multi-phase mixture which may include liquid and gaseous hydrocarbons, gaseous products of combustion, and condensed water. The water may be connate water originally present in the formation, water resulting from condensation of combustion products, or both. The presence of the several fluid phases in the formation greatly reduces the permeability of the formation to any one phase. As a result of these factors, often the resistance to flow is so high it is not possible to inject an oxygen-containing gas into a formation at rates high enough to allow economic production by a forward burning process or, in some instances, to maintain combustion.
An in-situ combustion method that has been developed for the production of heavy oils from formations such as tar sands is the reverse combustion process. In that process, an ox gen-containing gas is injected into the formation at the injection well and oil in the formation is ignited at an adjacent production well. The combustion front then moves from the production well towards the injection well. The oil produced by the process and the combustion products move in a direction opposite that of the combustion front and are discharged from the formation into the production well. In the reverse com- 3 .11345 Patented Nov. 12, 1%53 bustion process, the oil that is moved through the formation is hot and moves through a hot formation of increased permeability. Because of the lower viscosity of the hot oil and the increased permeability of the formation, the resistance to flow is much less than in the forward burning process. The conventional in-situ reverse combustion process is described in United States Letters Patent No. 2,793,696 of R. A. Morse.
The conventional reverse combustion process has an important disadvantage in that only a portion of the oil in the formation is burned or produced. The remainder of the oil is coked in place in the formation and is left in the formation as the combustion front moves to wards the injection well. The coke represents oil that cannot be recovered from the formation. The injection of additional air into the formation after the combustion front has moved to the injection well merely burns the coke in place and produces carbon monoxide, carbon dioxide, and water. In spite of this disadvantage of the reverse combustion process, in many oil-bearing formations of low permeability or containing heavy oils, or in some partially depleted formations, it is the only effective method of recovering oil from the pay zone.
This invention resides in a low temperature reverse combustion process in which oil in a fluid form remains in the pay zone after the combustion front has passed and that oil may then be recovered from the hot formation by an appropriate subsequent secondary recovery step. Reverse combustion of the low temperature type is maintained and the peak temperature is controlled within narrow limits by regulation of the flux of the oxygen-containing gas injected into the formation. The term flux refers to the rate of injection of the gas in terms of volume of gas injected per unit area of the combustion front per unit of time.
FIGURE 1 is a diagrammatic illustration of experimental apparatus set up to observe the in-situ combustion process of this invention.
FIGURE 2 is a diagrammatic sectional view of a well adapted to perform a low temperature reverse combustion process according to one embodiment of this invention.
FIGURE 3 is a graph in which the peak temperatures attained by tar sands during experimental runs are plotted against the air flux.
FIGURE 4 is a graph in which the percent of oil in the tar sand that was recovered by several experimental runs of in-situ combustion processes is plotted against the air flux.
FIGURE 5 is a graph in which the st-andmd cubic feet of air injected to recover a barrel of oil is plotted against air flux for several experimental runs.
The important advantage in the process of this invention resides in leaving a liquid residue in the oil-bearing formation after the reverse combustion step has been completed. The liquid residue being hot and in a hot formation can then be recovered by additional steps, for example, a forward combustion step, a gas repressuring operation, a water flood operation, or a fracture-gravity drainage step. The combination of low temperature reverse combustion with one of these additional recovery steps frequently gives rise to an improved process, with an improved oil recovery and improved over-ail economics. In particular, the combination of low temperature reverse combustion with forward combustion as a addition to the oil.
3 subsequent recovery step results in a process with a lower over-all air-oil ratio and hence better economics than could be obtained using conventional reverse combustion alone.
Whether or not the residue in the formation following the reverse combustion step is liquid depends upon the amount and extent of :coldng of the oil 1 it in the formation. The extent of coking in turn will depend on the temperature reached by the formation as the combustion front passes through it and the nature of the oil left in the formation.
It has been found that the peak temperature attained in the formation depends on the flux of the oxygen-containing gas. Experimental reverse combustion runs were made on tar sands from six different sources. Several diilerent oil saturations for the same tar sand were also used in different runs. In addition, runs were made when the tar sands had a relatively high water saturation in The experimental runs were made in test equipment using five diierent types of combustion chambers which included transite pipe inch thiclc with no external heaters, an insulated stainless steel pipe 5 inches in diameter with no external heater, and three 7 different stainless steel pipes 2 /2 inches in diameter with heating elements and controls of dilferen-t designs for temperature regulationp In spite of the Wide variations in the nature of the tar sands and the experimental apparatus, it has been found that the peak temperature attained by thetar sands can be controlled within narrow limits by control of the air flux alone.
Experimental runs showing the dependence of the peak temperature, oil recovery, and air to oil ratio attained in reverse combustion processes upon the air flux were performed in apparatus diagrammatically illustrated in 7 FIGURE 1 of the drawings. Referring to that figure, a compressed air container 1% is provided with a discharge line 32 in which there is a reducing valve 14 to control the pressure. A metering device v15, illustrated as a rotameter, in line 12 allows continuous measurement for control or" the rate of llow of the air. A line 18 connects the discharge end of the rotameter 16 with the inlet of a combustion tube indicated generally by reference numeral 22 through a pressure reducing valve 23-.
Combustion tube 22 illustrated in FZGURE 1 consists of a -central tube 24 closed at its upper end except for connection with line 1'8 and at its lower end except for connection with a discharge line 25. Tube 24- is surrounded with a thin layer of insulation 28 around which are assembled electrical heaters 36 supplied with electrical power leads 32.
A thermocouple 34 is positioned in the center of the combustion tube 2 by passing it through a thermocouple well 36 and a gas tight seal 38 located on the end of the thermocouple well 36. A thermocouple 4% is located with its junction on insulation 28 by passing it through a hole 42 in heater 30. An outer layer of insulation 44 encloses the complete combustion tube assembly 22.
Thermocouples 34 and 4t and power leads 32 are connected to a control system (not shown in FIGURE 1) in such a way that whenever thermocouple 34 is hotter than thermocouple 4% electrical current is supplied to V heater 3%, and whenever thermocouple 413 is hotter than thermocouple 34 electrical curernt is not supplied to heater 3% Furthermore, the controller is so designed that the rate of heat generated by the heater 3% is in proportion to the rate at which the temperature at the center of the tube is increasing. Controllers of this kind are well known to those versed in the art. For the purpose of maintaining the entire combustion tube 22 in a locally adiabatic condition, a series of individual heaters 3t each with its associated thermocouple pairs (34 and 46'), power leads 32, and proportional controllers, are provided along the length of the tube.
Discharge line 26 opens into the upper end of a separator 46. An outlet line 4% provided with a valve 5% allows 4 withdrawal or" liquid collected in the separator as. Gaseous products and entrained liquids from the separator as are delivered through a line 5'2 to the upper end of a condenser coil 5%. Cooling means illustrated as a water cooled jacket 56 around the condenser coil it cools the gases from separator is to a temperature at which the less volatile products of combustion will condense. The mixture of gas and liquid products from the condenser coil 54- is delivered through line 58 to a separator 60. Liquid products collected in separator 6%- are discharged through a line 62. provided with a valve 64. Uncondensed gaseous products from separator together with entrained liquids pass through a side outlet line 66 into the bottom of a high voltage electrical preoipitator as where entrained liquids are removed from the gases and drain through a discharge line 7% into a receiver '72. Liquid products collected in receiver 72 are discharged through a line 74 provided with a valve '75. Gaseous products are discharged from the top of the electrical precipitator through a line 78 into a gas meter 39 which measures the how rate of non-co-nde-nsible gaseous products from precipitator 6-8. Gaseous products from the gas meter 8% are discharged to the atmosphere through line 82.
In preparation for each of the experimental runs, suitably sized rods were insented through thermocouple wells 36 flush with the inside wall of the combustion tube 24 and one end plate was bolted in position to close one end of the tube. Heating'elements 36 were turned on and the entire tube heated to about 200 F. Tar sand was preheated to 200 F. and carefully tamped in place until the tube 24- was full. The other end plate was bolted in position and the rods in the thermocouple wells were driven into the center of the sand and then removed. Thermocouples 34 were inserted through the thermocouple wells 38 and into the center of the sand thus occupying the space created by removal of the rods. The complete assembly 22 was then allowed to cool to room temperature.
With the tube in a Vertical position an electric flange heater 84 is heated as rapidly as possible to a temperature sufiiciently high to initiate combustion at the air flux used. When this temperature is reached, air is admitted to the tube 24 through the line 18 at the do sired rate. Immediately upon contact of the air with the hot tar sand at the bottom 'of the tube combustion is initiated, and a combustion zone is formed and moves from the bottom to the top of the tube.
At this time there will still be warm oil remaining in the sand in a quantity which depends on the air flux used. The lower the flux used, the greater Will be the amount of oil remaining. This oil can then be recovered by a variety of subsequent recovery steps mentioned earlier. However, in the case of the data which will be presented, this oil was recovered by forward combustion. Thus, in case the remaining oil is to be recovered by forward combustion, air is injected in the top of t b 22 through line 18 at a rate suitable to the economic P duction of oil by that process. This rateneed not "be the same as that used for the low temperature reverse combustion operation, but as a matter of convenience, it was the same in the experiments which will be reported. Following the forward combustion step; only a clean sand remains in the combustion tube, all hydrocarbon material having been either recovered or burned in the improved process.
The procedure indicated above was repeated for tar sands from six sources. The curve presented in FIG- URE 3 of the drawings is an average of the peak temperatures achieved during twenty of these runs carried out at various values of the air flux and for tar sands from several sources. The data obtained on experimental runs on tar sands fromseveral sources are presented in Table 1. Similar results are obtained when the tube 24 is packed with crushed oil shale.
Table 1 Oil Satura- Air Flux,
tion, Wt. s.c.f./(hr.) Average Tar Sand Percent (ft. Peak Based 011 Based on Temp,
Original Empty F. tar sand Tube Asphalt Ridge 12. 4 41. 3 742 D 11. 9 72. 3 928 Do. 12.6 72.3 929 Do. 11.9 72. 3 981 Do 11.8 72.3 963 Oklahoma 8. 0 71. 3 903 Do 8.0 35. 5 716 VernaL. 7. 4 44. 3 760 Do 7. 2 53. 7 879 Athabaska 13. 2 53. 0 861 D 12.6 13. 2 565 UVa1de 18. 7 53. 9 858 stile-basin..." l3. 1 134 1, 030 Dismal Crceln- 8. 2 50.8 899 Athabaska 13. 1 55. 3 888 11. 4 75. 3 882 12. 2 40.1 726 11. 4 38.1 733 ll. 2 24.1 610 13.0 9. 20 500 It was found that if the peak temperature reached during the reverse combustion process did not exceed 75 0 F., that additional liquid hydrocarbon product was obtained upon injection of air after the reverse combustion had proceeded from the outlet to the inlet end of the tar sand.
The plot of the percent of oil recovered against the air flux in FIGURE 4 shows the advantages of this invention in causing increased recovery of oil. The dotted line to the left of the intersection of the lines in FIG- URE 4 indicates the total recovery of oil and the solid line to the left of the intersection indicates the recovery during the low temperature reverse combustion step. It will be noted that at air fluxes causing temperatures below about 759 F. (corresponding to fluxes of about 40 standard cubic feet per square foot per hour) additional oil was recovered upon injection of air after reverse combustion had ceased. In the run at the air flux of approximately 9 standard cubic feet per square foot per hour, the recovery was increased from 17% to 59% of the oil in the tar sand. In contrast, in runs at air fluxes in excess of 40 standard cubic feet per square foot per hour, no additional oil was recovered after the reverse combustion had proceeded from the outlet to the inlet end of the combustion tubing.
Another advantage of this invention is shown in FIG- URE 5, where the ratio of air injected to oil recovered is plotted against the air flux. The dotted line to the left of the intersection of the lines in FIGURE 5 indicates the over-all air-oil ratio for a process consisting of low temperature reverse combustion followed by a forward combustion step. The solid line to the left of the intersection of the lines in FIGURE 5 indicates the air-oil ratio during the low temperature reverse combustion step. it will be noted that at air fluxes causing temperatures below about 750 F. (corresponding to fluxes of about 40 standard cubic feet per square foot per hour) upon injection of air after reverse combustion had ceased, a sufficiently large decrease in the -air-oil ratio was obtained that the over-all air-oil ratio was lower than could ever be achieved by a recovery process wherein the first step was conventional reverse combustion.
The curve in FIGURE 3 shows the relation between the peak temperature attained and the air flux at substantially atmospheric pressure. Higher pressures result in lower peak temperatures for a given air flux. For example, an air flux of 55 standard cubic feet per square foot per :hour passed through a tar sand under a pressure of 450 pounds per square inch, resulted in 'a peak temperature of 550 F. At atmospheric pressure the same air flux would result in a temperature of approximately 855 F. However, an air flux less than 40 standard cubic feet per square foot per hour in a reverse combustion 6 process would allow recovery of additional oil from the formation after the reverse combustion process is completed in a reverse combustion process performed at high pressures as well as low pressures because of the lower peak temperatures reached.
One well structure adapted for carrying out the process of this invention is illustrated in FIGURE 2 of the drawings. Referring to that figure, a well indicated generally by reference numeral is drilled through an oil-bearing formation 92 between a cap rock 94 and an underlying base rock 96 to a total depth 98. Casing 1% is run into the well and cemented in place by a sheath 1492 of cement in accordance with the usual techniques for thermal recovery processes. The casing 160 and cement sheath 102 are perforated at 104 near the upper limits of the pay zone 92 and at 106 near the bottom of the pay Zone.
A large substantially horizontal radial fracture 108 is made in the lower portion of the pay Zone. A similar fracture 114 is made near the upper limit of the pay zone. A packer 112 is run into the casing 1% and set at a position between the upper perforations 104 and lower perforations i496. Tubing 114 extends from the well head through packer 112 and opens at its lower end within the casing adjacent the perforations 106. Tubing 114 extends upwardly through a cap 116 closing the upper end of the well and is connected with a line 118 for delivery of oil produced from the well. An air supply line 129 extends through the cap 116 and communicates with the annular space 122 between the casing 10% and the tubing 114.
In carrying out the process of this invention, a suitable burner, not shown, is positioned in the well adjacent the perforations 1%. A mixture of a fuel and air is burned adjacent the perforations 1G6 and the products of combustion forced into the fracture 11% to heat the formation around fracture 108 to a temperature high enough to initiate reverse combustion. Air is introduced into the well through line and discharged through perforations 164 into fracture 110. The air flows downwardly through the pay zone 92 to cause in-situ combustion of oil to begin in the hot formation adjacent the fracture 1&8. As the injection of air is continued, the combustion front moves upwardly countercurrent to the flow of air, and oil produced from the formation is removed through line 114. injection of air is continued at a rate controlled to maintain the temperature in the formation below 750 F. The substantially linear flow from the upper fracture to the lower fracture facilitates control of the air flux. When the combustion front reaches the upper fracture 110, the flow of air can be stopped and production of the hot oil remaining in the formation obtained by a gas repressuring process, a water injection process, or by gravity drainage. It is preferred, however, to follow the low temperature reverse combustion step by a forward combustion process by injection of additional air, thus effectively removing substantially all of the remaining oil from the heated pay zone. Any gravity drainage that may occur in the pay zone favors increased recovery of the oil when the production is delivered into the lower fracture during both the low temperature reverse combustion and subsequent recovery steps. The fractures through which air is injected and the production recovered can be reversed, but the advantage of gravity drainage is not obtained if the direction of flow is reversed.
Ignition of oil in the formation is accomplished by heating the formation to a temperature sufficiently high that when contacted with an oxygen-containing gas ignition will occur. A preferred method is to inject air into the formation at the injection well until it can be produced at the production Well with an oxygen content high enough to cause ignition of oil in the formation when the formation is heated. Air injection is then stopped and a gas burner ignited in the production well. The products of combustion are displaced into the formation until the formation is heated-for a radial distance of at least a few inches from the borehole of the production well to a temperature higher than the peak temperature attained in a low temperature reverse combustion process at the air fiux existing in the heated zone when air injection is resumed. The burner is then removed from the production well and air again injected into the formation at the injection well. Ignition occurs as air reaches the heated zone in the formation.
If an electric heater is used, the formation surrounding the production well is heated by conduction or by gases passed over the heater and into the formation. If air is passed over the electric heater, forward combustion may be initiated at the production well. Forward combustion can be continued until an injection pressure approaching the overburden pressure on the formation is attained. The injection of air at the production well is then stopped and air is injected at the injection well. When the air from the injection well reaches the zone of forward combustion, the combustion is converted to reverse combustion. After reverse combustion has started, the air flux is adjusted to cause the desired flow temperature reverse combustion.
The process of this invention can be used in other well arrangements. For example, one well may be used as an input well and an adjacent well as a production well. Another arrangement that can be used effectively is to use wells in one row as injection wells and in an adjacent row as production wells. The location at which oil is delivered from the formation in channels for delivery to the well head and recovery is generally referred to as the production wellin the description of this invention. it is to be understood that the invention is not limited to a process using separate injection and production wells and that the term production well includes within its scope any production zone spaced from the injection zone through which oil is produced from the formation into channels suitable for delivery of the oil, gas, and combustion products to the well head.
In a specific example of the production of oil by this invention, a well is drilled to a total depth of 575 feet through a pay zone in the interval of 530 to 565 feet. Casing is run into the well to total depth and cemented by conventional practice. The casing and surrounding cement sheath are then severed by a ring shaped charge at a depth of 560 feet and again at a depth of 535 feet. A packer is set in the casing between the two levels at which the casing is cut. The formation is then fractured through the lower opening in the casing to form a horizontal fracture having an estimated radius of 100 feet, and the fracture is propped open with coarse sand. With the packer in place but closed to isolate the lower fracture, a horizontal fracture having an estimated radius of 100 feet is formed through the opening in the casing at a depth of 535 feet. The upper fracture is also propped open with coarse sand.
A burner is run through the packer to a position adjacent the lower fracture and a combustible mixture of lease gas and air delivered to the burner at a rate of 2000 cubic feet of lease gas per hour and burned below the packer. The hot products of combustion are displaced from the borehole into the lower fracture to heat the formation adjacent the fracture to a temperature estimated to range between 1060" F. and 750 F. The burner is pulled from the hole and tubing run through j the packer to a position with its lower end opening adja- 'ly to the upper fracture.
cent the lower fracture.
Air is then displaced into the upper fracture at a rate of 600,609 standard cubic feet per hour causin an air flux of approximately 20 standard cubic feet per square foot per hour at the combustion front between the upper and lower fracture. When the air contacts the heated formation, low temperature reverse combustion of the oil in the formation is initiated. The injection of air is continued to cause the combustion front'to move upward- A mixture of hot oil, gas, and combustion products is delivered through the bottom fracture into the borehole and lifted through the tubing to the well head.
The process of this invention results in the production of an oil of relatively low specific gravity. The production of low specific gravity oil during the low temperature reverse combustion process is believed to be attributable to an eficient fractionation of light ends out of the oil by the advancing thermal wave in conjunction with the predominantly inert gas atmosphereprovided by the nitrogen content of injected air together with products of combustion which are accumulating in concentration the temperature increases. The oil produced in the low temperature reverse combustion is frequently clear and amber in color rather than the dark oil produced in the reverse combustion processes of the prior art.
In the specification and claim of this application, the term low temperature reverse combustion is used to designate a reverse combustion process in which the peak temperature is low enough that fluid oil remains in the formation after completion of the reverse combustion process. That fluid oil is hot and can then be recovered from the hot formation in a subsequent recovery step and thereby increase the amount of oil recovered from the formation.
We claim:
An in-situ combustion process for the recovery of oil from an oil-bearing subsurface formation penetrated by an injection well and a production well spaced from the injection well, comprising displam'ng air down the injection well into the oil-bearing formation and through the oil-bearing formation to the production well, heating oil in the oil-bearing formation adjacent the production well to a temperature whereby said oil ignites upon contact with the air displaced through the formation, continuing the displacement of air into the formation at a rate controlled to give an air flux at the combustion front less than about 40 std. cut. ft./sq. ft./hr. to cause reverse combustion to proceed at a temperature below approximately 750 F. from the production well to the injection well, discontinuing the displacement of air down the injection well and into the formation upon arrival of the reverse combustion front at the injection well, thereafter displacing water down the injection well and into the formation to drive oil present in the formation to the production well, and lifting oil through the production Well to the surface.
References Cited in the file of this patent UNITED STATES PATENTS 2,793,696 Morse Ma /28, 1957 2,819,761 .Popham et al. Jan. 14, 1958 2,853,137 Marx 'Sept, 23, 1958 2,889,881 Trantharn et al. June 9, 1959
US795636A 1959-02-26 1959-02-26 Low temperature reverse combustion process Expired - Lifetime US3110345A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
US795636A US3110345A (en) 1959-02-26 1959-02-26 Low temperature reverse combustion process

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US795636A US3110345A (en) 1959-02-26 1959-02-26 Low temperature reverse combustion process

Publications (1)

Publication Number Publication Date
US3110345A true US3110345A (en) 1963-11-12

Family

ID=25166059

Family Applications (1)

Application Number Title Priority Date Filing Date
US795636A Expired - Lifetime US3110345A (en) 1959-02-26 1959-02-26 Low temperature reverse combustion process

Country Status (1)

Country Link
US (1) US3110345A (en)

Cited By (44)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3196945A (en) * 1962-10-08 1965-07-27 Pan American Petroleum Company Method of forward in situ combustion with water injection
US3205944A (en) * 1963-06-14 1965-09-14 Socony Mobil Oil Co Inc Recovery of hydrocarbons from a subterranean reservoir by heating
US3221809A (en) * 1963-06-14 1965-12-07 Socony Mobil Oil Co Inc Method of heating a subterranean reservoir containing hydrocarbon material
US3239405A (en) * 1963-11-04 1966-03-08 Pan American Petroleum Corp Underground combustion process
US3280910A (en) * 1964-03-20 1966-10-25 Mobil Oil Corp Heating of a subterranean formation
US3334687A (en) * 1964-09-28 1967-08-08 Phillips Petroleum Co Reverse in situ combustion process for the recovery of oil
US3385362A (en) * 1966-10-26 1968-05-28 Mobil Oil Corp Thermal recovery of viscous oil with selectively spaced fractures
US3451478A (en) * 1965-11-01 1969-06-24 Pan American Petroleum Corp Nuclear fracturing and heating in water flooding
WO2001081240A2 (en) * 2000-04-24 2001-11-01 Shell Internationale Research Maatschappij B.V. In-situ heating of coal formation to produce fluid
US20030079877A1 (en) * 2001-04-24 2003-05-01 Wellington Scott Lee In situ thermal processing of a relatively impermeable formation in a reducing environment
US20030080604A1 (en) * 2001-04-24 2003-05-01 Vinegar Harold J. In situ thermal processing and inhibiting migration of fluids into or out of an in situ oil shale formation
US20030098149A1 (en) * 2001-04-24 2003-05-29 Wellington Scott Lee In situ thermal recovery from a relatively permeable formation using gas to increase mobility
US6588504B2 (en) 2000-04-24 2003-07-08 Shell Oil Company In situ thermal processing of a coal formation to produce nitrogen and/or sulfur containing formation fluids
US20030173081A1 (en) * 2001-10-24 2003-09-18 Vinegar Harold J. In situ thermal processing of an oil reservoir formation
US20030173085A1 (en) * 2001-10-24 2003-09-18 Vinegar Harold J. Upgrading and mining of coal
US20030196810A1 (en) * 2001-10-24 2003-10-23 Vinegar Harold J. Treatment of a hydrocarbon containing formation after heating
US6698515B2 (en) 2000-04-24 2004-03-02 Shell Oil Company In situ thermal processing of a coal formation using a relatively slow heating rate
US6715548B2 (en) 2000-04-24 2004-04-06 Shell Oil Company In situ thermal processing of a hydrocarbon containing formation to produce nitrogen containing formation fluids
US6715546B2 (en) 2000-04-24 2004-04-06 Shell Oil Company In situ production of synthesis gas from a hydrocarbon containing formation through a heat source wellbore
US20050269091A1 (en) * 2004-04-23 2005-12-08 Guillermo Pastor-Sanz Reducing viscosity of oil for production from a hydrocarbon containing formation
US7011154B2 (en) 2000-04-24 2006-03-14 Shell Oil Company In situ recovery from a kerogen and liquid hydrocarbon containing formation
US7066254B2 (en) 2001-04-24 2006-06-27 Shell Oil Company In situ thermal processing of a tar sands formation
US7073578B2 (en) 2002-10-24 2006-07-11 Shell Oil Company Staged and/or patterned heating during in situ thermal processing of a hydrocarbon containing formation
US7090013B2 (en) 2001-10-24 2006-08-15 Shell Oil Company In situ thermal processing of a hydrocarbon containing formation to produce heated fluids
US7096953B2 (en) 2000-04-24 2006-08-29 Shell Oil Company In situ thermal processing of a coal formation using a movable heating element
US7104319B2 (en) 2001-10-24 2006-09-12 Shell Oil Company In situ thermal processing of a heavy oil diatomite formation
US7121342B2 (en) 2003-04-24 2006-10-17 Shell Oil Company Thermal processes for subsurface formations
US7165615B2 (en) 2001-10-24 2007-01-23 Shell Oil Company In situ recovery from a hydrocarbon containing formation using conductor-in-conduit heat sources with an electrically conductive material in the overburden
US20070045265A1 (en) * 2005-04-22 2007-03-01 Mckinzie Billy J Ii Low temperature barriers with heat interceptor wells for in situ processes
US20070095536A1 (en) * 2005-10-24 2007-05-03 Vinegar Harold J Cogeneration systems and processes for treating hydrocarbon containing formations
US20080038144A1 (en) * 2006-04-21 2008-02-14 Maziasz Phillip J High strength alloys
US20080128134A1 (en) * 2006-10-20 2008-06-05 Ramesh Raju Mudunuri Producing drive fluid in situ in tar sands formations
US20090071652A1 (en) * 2007-04-20 2009-03-19 Vinegar Harold J In situ heat treatment from multiple layers of a tar sands formation
US20090189617A1 (en) * 2007-10-19 2009-07-30 David Burns Continuous subsurface heater temperature measurement
US20090260823A1 (en) * 2008-04-18 2009-10-22 Robert George Prince-Wright Mines and tunnels for use in treating subsurface hydrocarbon containing formations
US20100089584A1 (en) * 2008-10-13 2010-04-15 David Booth Burns Double insulated heaters for treating subsurface formations
US8327932B2 (en) 2009-04-10 2012-12-11 Shell Oil Company Recovering energy from a subsurface formation
US8631866B2 (en) 2010-04-09 2014-01-21 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
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 (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2793696A (en) * 1954-07-22 1957-05-28 Pan American Petroleum Corp Oil recovery by underground combustion
US2819761A (en) * 1956-01-19 1958-01-14 Continental Oil Co Process of removing viscous oil from a well bore
US2853137A (en) * 1956-05-14 1958-09-23 Phillips Petroleum Co Oil recovery by in situ-combustion
US2889881A (en) * 1956-05-14 1959-06-09 Phillips Petroleum Co Oil recovery by in situ combustion

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2793696A (en) * 1954-07-22 1957-05-28 Pan American Petroleum Corp Oil recovery by underground combustion
US2819761A (en) * 1956-01-19 1958-01-14 Continental Oil Co Process of removing viscous oil from a well bore
US2853137A (en) * 1956-05-14 1958-09-23 Phillips Petroleum Co Oil recovery by in situ-combustion
US2889881A (en) * 1956-05-14 1959-06-09 Phillips Petroleum Co Oil recovery by in situ combustion

Cited By (365)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3196945A (en) * 1962-10-08 1965-07-27 Pan American Petroleum Company Method of forward in situ combustion with water injection
US3205944A (en) * 1963-06-14 1965-09-14 Socony Mobil Oil Co Inc Recovery of hydrocarbons from a subterranean reservoir by heating
US3221809A (en) * 1963-06-14 1965-12-07 Socony Mobil Oil Co Inc Method of heating a subterranean reservoir containing hydrocarbon material
US3239405A (en) * 1963-11-04 1966-03-08 Pan American Petroleum Corp Underground combustion process
US3280910A (en) * 1964-03-20 1966-10-25 Mobil Oil Corp Heating of a subterranean formation
US3334687A (en) * 1964-09-28 1967-08-08 Phillips Petroleum Co Reverse in situ combustion process for the recovery of oil
US3451478A (en) * 1965-11-01 1969-06-24 Pan American Petroleum Corp Nuclear fracturing and heating in water flooding
US3385362A (en) * 1966-10-26 1968-05-28 Mobil Oil Corp Thermal recovery of viscous oil with selectively spaced fractures
US6871707B2 (en) 2000-04-24 2005-03-29 Shell Oil Company In situ thermal processing of a hydrocarbon containing formation with carbon dioxide sequestration
US6729396B2 (en) 2000-04-24 2004-05-04 Shell Oil Company In situ thermal processing of a coal formation to produce hydrocarbons having a selected carbon number range
US7798221B2 (en) 2000-04-24 2010-09-21 Shell Oil Company 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
US7096953B2 (en) 2000-04-24 2006-08-29 Shell Oil Company In situ thermal processing of a coal formation using a movable heating element
US7096941B2 (en) 2000-04-24 2006-08-29 Shell Oil Company In situ thermal processing of a coal formation with heat sources located at an edge of a coal layer
US7086468B2 (en) 2000-04-24 2006-08-08 Shell Oil Company In situ thermal processing of a hydrocarbon containing formation using heat sources positioned within open wellbores
US7036583B2 (en) 2000-04-24 2006-05-02 Shell Oil Company In situ thermal processing of a hydrocarbon containing formation to increase a porosity of the formation
US6581684B2 (en) 2000-04-24 2003-06-24 Shell Oil Company In Situ thermal processing of a hydrocarbon containing formation to produce sulfur containing formation fluids
US7017661B2 (en) 2000-04-24 2006-03-28 Shell Oil Company Production of synthesis gas from a coal formation
US6588504B2 (en) 2000-04-24 2003-07-08 Shell Oil Company In situ thermal processing of a coal formation to produce nitrogen and/or sulfur containing formation fluids
US6591907B2 (en) 2000-04-24 2003-07-15 Shell Oil Company In situ thermal processing of a coal formation with a selected vitrinite reflectance
US6591906B2 (en) 2000-04-24 2003-07-15 Shell Oil Company In situ thermal processing of a hydrocarbon containing formation with a selected oxygen content
US7011154B2 (en) 2000-04-24 2006-03-14 Shell Oil Company In situ recovery from a kerogen and liquid hydrocarbon containing formation
US6997255B2 (en) 2000-04-24 2006-02-14 Shell Oil Company In situ thermal processing of a hydrocarbon containing formation in a reducing environment
US6994161B2 (en) 2000-04-24 2006-02-07 Kevin Albert Maher In situ thermal processing of a coal formation with a selected moisture content
US6994168B2 (en) * 2000-04-24 2006-02-07 Scott Lee Wellington In situ thermal processing of a hydrocarbon containing formation with a selected hydrogen to carbon ratio
US6994160B2 (en) 2000-04-24 2006-02-07 Shell Oil Company In situ thermal processing of a hydrocarbon containing formation to produce hydrocarbons having a selected carbon number range
US6991031B2 (en) 2000-04-24 2006-01-31 Shell Oil Company In situ thermal processing of a coal formation to convert a selected total organic carbon content into hydrocarbon products
US6973967B2 (en) 2000-04-24 2005-12-13 Shell Oil Company Situ thermal processing of a coal formation using pressure and/or temperature control
US8789586B2 (en) 2000-04-24 2014-07-29 Shell Oil Company In situ recovery from a hydrocarbon containing formation
US6889769B2 (en) 2000-04-24 2005-05-10 Shell Oil Company In situ thermal processing of a hydrocarbon containing formation with a selected moisture content
US6966372B2 (en) 2000-04-24 2005-11-22 Shell Oil Company In situ thermal processing of a hydrocarbon containing formation to produce oxygen containing formation fluids
US6959761B2 (en) 2000-04-24 2005-11-01 Shell Oil Company In situ thermal processing of a coal formation with a selected ratio of heat sources to production wells
US6607033B2 (en) 2000-04-24 2003-08-19 Shell Oil Company In Situ thermal processing of a coal formation to produce a condensate
US6609570B2 (en) 2000-04-24 2003-08-26 Shell Oil Company In situ thermal processing of a coal formation and ammonia production
US6953087B2 (en) 2000-04-24 2005-10-11 Shell Oil Company Thermal processing of a hydrocarbon containing formation to increase a permeability of the formation
US6948563B2 (en) 2000-04-24 2005-09-27 Shell Oil Company In situ thermal processing of a hydrocarbon containing formation with a selected hydrogen content
US6923258B2 (en) 2000-04-24 2005-08-02 Shell Oil Company In situ thermal processsing of a hydrocarbon containing formation to produce a mixture with a selected hydrogen content
US6913078B2 (en) 2000-04-24 2005-07-05 Shell Oil Company In Situ thermal processing of hydrocarbons within a relatively impermeable formation
US6910536B2 (en) 2000-04-24 2005-06-28 Shell Oil Company In situ thermal processing of a hydrocarbon containing formation using a natural distributed combustor
US6688387B1 (en) 2000-04-24 2004-02-10 Shell Oil Company In situ thermal processing of a hydrocarbon containing formation to produce a hydrocarbon condensate
US6698515B2 (en) 2000-04-24 2004-03-02 Shell Oil Company In situ thermal processing of a coal formation using a relatively slow heating rate
US6902004B2 (en) 2000-04-24 2005-06-07 Shell Oil Company In situ thermal processing of a hydrocarbon containing formation using a movable heating element
US6702016B2 (en) 2000-04-24 2004-03-09 Shell Oil Company In situ thermal processing of a hydrocarbon containing formation with heat sources located at an edge of a formation layer
US6708758B2 (en) 2000-04-24 2004-03-23 Shell Oil Company In situ thermal processing of a coal formation leaving one or more selected unprocessed areas
US6712136B2 (en) 2000-04-24 2004-03-30 Shell Oil Company In situ thermal processing of a hydrocarbon containing formation using a selected production well spacing
US6712137B2 (en) 2000-04-24 2004-03-30 Shell Oil Company In situ thermal processing of a coal formation to pyrolyze a selected percentage of hydrocarbon material
US6712135B2 (en) 2000-04-24 2004-03-30 Shell Oil Company In situ thermal processing of a coal formation in reducing environment
US6715548B2 (en) 2000-04-24 2004-04-06 Shell Oil Company In situ thermal processing of a hydrocarbon containing formation to produce nitrogen containing formation fluids
US6715549B2 (en) 2000-04-24 2004-04-06 Shell Oil Company In situ thermal processing of a hydrocarbon containing formation with a selected atomic oxygen to carbon ratio
US6715546B2 (en) 2000-04-24 2004-04-06 Shell Oil Company In situ production of synthesis gas from a hydrocarbon containing formation through a heat source wellbore
US6715547B2 (en) 2000-04-24 2004-04-06 Shell Oil Company In situ thermal processing of a hydrocarbon containing formation to form a substantially uniform, high permeability formation
US6719047B2 (en) 2000-04-24 2004-04-13 Shell Oil Company In situ thermal processing of a hydrocarbon containing formation in a hydrogen-rich environment
US6722429B2 (en) 2000-04-24 2004-04-20 Shell Oil Company In situ thermal processing of a hydrocarbon containing formation leaving one or more selected unprocessed areas
US6722431B2 (en) 2000-04-24 2004-04-20 Shell Oil Company In situ thermal processing of hydrocarbons within a relatively permeable formation
US6722430B2 (en) 2000-04-24 2004-04-20 Shell Oil Company In situ thermal processing of a coal formation with a selected oxygen content and/or selected O/C ratio
US6725928B2 (en) 2000-04-24 2004-04-27 Shell Oil Company In situ thermal processing of a coal formation using a distributed combustor
US6725920B2 (en) 2000-04-24 2004-04-27 Shell Oil Company In situ thermal processing of a hydrocarbon containing formation to convert a selected amount of total organic carbon into hydrocarbon products
US6725921B2 (en) 2000-04-24 2004-04-27 Shell Oil Company In situ thermal processing of a coal formation by controlling a pressure of the formation
US6729401B2 (en) 2000-04-24 2004-05-04 Shell Oil Company In situ thermal processing of a hydrocarbon containing formation and ammonia production
US6729395B2 (en) 2000-04-24 2004-05-04 Shell Oil Company In situ thermal processing of a hydrocarbon containing formation with a selected ratio of heat sources to production wells
US6729397B2 (en) 2000-04-24 2004-05-04 Shell Oil Company In situ thermal processing of a hydrocarbon containing formation with a selected vitrinite reflectance
US6902003B2 (en) 2000-04-24 2005-06-07 Shell Oil Company In situ thermal processing of a hydrocarbon containing formation having a selected total organic carbon content
US6732795B2 (en) 2000-04-24 2004-05-11 Shell Oil Company In situ thermal processing of a hydrocarbon containing formation to pyrolyze a selected percentage of hydrocarbon material
US6732796B2 (en) 2000-04-24 2004-05-11 Shell Oil Company In situ production of synthesis gas from a hydrocarbon containing formation, the synthesis gas having a selected H2 to CO ratio
US6732794B2 (en) 2000-04-24 2004-05-11 Shell Oil Company In situ thermal processing of a hydrocarbon containing formation to produce a mixture with a selected hydrogen content
US6736215B2 (en) 2000-04-24 2004-05-18 Shell Oil Company In situ thermal processing of a hydrocarbon containing formation, in situ production of synthesis gas, and carbon dioxide sequestration
US6739394B2 (en) 2000-04-24 2004-05-25 Shell Oil Company Production of synthesis gas from a hydrocarbon containing formation
US6739393B2 (en) 2000-04-24 2004-05-25 Shell Oil Company In situ thermal processing of a coal formation and tuning production
US6742593B2 (en) 2000-04-24 2004-06-01 Shell Oil Company In situ thermal processing of a hydrocarbon containing formation using heat transfer from a heat transfer fluid to heat the formation
US6742587B2 (en) 2000-04-24 2004-06-01 Shell Oil Company In situ thermal processing of a coal formation to form a substantially uniform, relatively high permeable formation
US6742589B2 (en) 2000-04-24 2004-06-01 Shell Oil Company In situ thermal processing of a coal formation using repeating triangular patterns of heat sources
US6742588B2 (en) 2000-04-24 2004-06-01 Shell Oil Company In situ thermal processing of a hydrocarbon containing formation to produce formation fluids having a relatively low olefin content
US6745832B2 (en) 2000-04-24 2004-06-08 Shell Oil Company Situ thermal processing of a hydrocarbon containing formation to control product composition
US6745837B2 (en) 2000-04-24 2004-06-08 Shell Oil Company In situ thermal processing of a hydrocarbon containing formation using a controlled heating rate
US6745831B2 (en) 2000-04-24 2004-06-08 Shell Oil Company In situ thermal processing of a hydrocarbon containing formation by controlling a pressure of the formation
US6749021B2 (en) 2000-04-24 2004-06-15 Shell Oil Company In situ thermal processing of a coal formation using a controlled heating rate
US6752210B2 (en) 2000-04-24 2004-06-22 Shell Oil Company In situ thermal processing of a coal formation using heat sources positioned within open wellbores
US6758268B2 (en) 2000-04-24 2004-07-06 Shell Oil Company In situ thermal processing of a hydrocarbon containing formation using a relatively slow heating rate
US6761216B2 (en) 2000-04-24 2004-07-13 Shell Oil Company In situ thermal processing of a coal formation to produce hydrocarbon fluids and synthesis gas
US6763886B2 (en) 2000-04-24 2004-07-20 Shell Oil Company In situ thermal processing of a coal formation with carbon dioxide sequestration
US6769483B2 (en) 2000-04-24 2004-08-03 Shell Oil Company In situ thermal processing of a hydrocarbon containing formation using conductor in conduit heat sources
US6769485B2 (en) 2000-04-24 2004-08-03 Shell Oil Company In situ production of synthesis gas from a coal formation through a heat source wellbore
US6789625B2 (en) 2000-04-24 2004-09-14 Shell Oil Company In situ thermal processing of a hydrocarbon containing formation using exposed metal heat sources
US6805195B2 (en) 2000-04-24 2004-10-19 Shell Oil Company In situ thermal processing of a hydrocarbon containing formation to produce hydrocarbon fluids and synthesis gas
US6896053B2 (en) 2000-04-24 2005-05-24 Shell Oil Company In situ thermal processing of a hydrocarbon containing formation using repeating triangular patterns of heat sources
WO2001081240A3 (en) * 2000-04-24 2002-07-04 Shell Oil Co In-situ heating of coal formation to produce fluid
US6820688B2 (en) 2000-04-24 2004-11-23 Shell Oil Company In situ thermal processing of coal formation with a selected hydrogen content and/or selected H/C ratio
US6866097B2 (en) 2000-04-24 2005-03-15 Shell Oil Company In situ thermal processing of a coal formation to increase a permeability/porosity of the formation
WO2001081240A2 (en) * 2000-04-24 2001-11-01 Shell Internationale Research Maatschappij B.V. In-situ heating of coal formation to produce fluid
US6877554B2 (en) 2000-04-24 2005-04-12 Shell Oil Company In situ thermal processing of a hydrocarbon containing formation using pressure and/or temperature control
US8485252B2 (en) 2000-04-24 2013-07-16 Shell Oil Company In situ recovery from a hydrocarbon containing formation
US6880635B2 (en) 2000-04-24 2005-04-19 Shell Oil Company In situ production of synthesis gas from a coal formation, the synthesis gas having a selected H2 to CO ratio
US20030142964A1 (en) * 2001-04-24 2003-07-31 Wellington Scott Lee In situ thermal processing of an oil shale formation using a controlled heating rate
US6951247B2 (en) 2001-04-24 2005-10-04 Shell Oil Company In situ thermal processing of an oil shale formation using horizontal heat sources
US20030141068A1 (en) * 2001-04-24 2003-07-31 Pierre De Rouffignac Eric In situ thermal processing through an open wellbore in an oil shale formation
US20040211557A1 (en) * 2001-04-24 2004-10-28 Cole Anthony Thomas Conductor-in-conduit heat sources for in situ thermal processing of an oil shale formation
US7032660B2 (en) * 2001-04-24 2006-04-25 Shell Oil Company In situ thermal processing and inhibiting migration of fluids into or out of an in situ 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
US20030079877A1 (en) * 2001-04-24 2003-05-01 Wellington Scott Lee In situ thermal processing of a relatively impermeable formation in a reducing environment
US20030080604A1 (en) * 2001-04-24 2003-05-01 Vinegar Harold J. In situ thermal processing and inhibiting migration of fluids into or out of an in situ oil shale formation
US6915850B2 (en) 2001-04-24 2005-07-12 Shell Oil Company In situ thermal processing of an oil shale formation having permeable and impermeable sections
US6918442B2 (en) 2001-04-24 2005-07-19 Shell Oil Company In situ thermal processing of an oil shale formation in a reducing environment
US6918443B2 (en) 2001-04-24 2005-07-19 Shell Oil Company In situ thermal processing of an oil shale formation to produce hydrocarbons having a selected carbon number range
US6880633B2 (en) 2001-04-24 2005-04-19 Shell Oil Company In situ thermal processing of an oil shale formation to produce a desired product
US6923257B2 (en) 2001-04-24 2005-08-02 Shell Oil Company In situ thermal processing of an oil shale formation to produce a condensate
US6929067B2 (en) 2001-04-24 2005-08-16 Shell Oil Company Heat sources with conductive material for in situ thermal processing of an oil shale formation
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
US8608249B2 (en) 2001-04-24 2013-12-17 Shell Oil Company In situ thermal processing of an oil shale formation
US6948562B2 (en) 2001-04-24 2005-09-27 Shell Oil Company Production of a blending agent using an in situ thermal process in a relatively permeable formation
US20030111223A1 (en) * 2001-04-24 2003-06-19 Rouffignac Eric Pierre De In situ thermal processing of an oil shale formation using horizontal heat sources
US7013972B2 (en) 2001-04-24 2006-03-21 Shell Oil Company In situ thermal processing of an oil shale formation using a natural distributed combustor
US20030146002A1 (en) * 2001-04-24 2003-08-07 Vinegar Harold J. Removable heat sources for in situ thermal processing of an oil shale formation
US6964300B2 (en) 2001-04-24 2005-11-15 Shell Oil Company In situ thermal recovery from a relatively permeable formation with backproduction through a heater wellbore
US6966374B2 (en) 2001-04-24 2005-11-22 Shell Oil Company In situ thermal recovery from a relatively permeable formation using gas to increase mobility
US20030148894A1 (en) * 2001-04-24 2003-08-07 Vinegar Harold J. In situ thermal processing of an oil shale formation using a natural distributed combustor
US7096942B1 (en) 2001-04-24 2006-08-29 Shell Oil Company In situ thermal processing of a relatively permeable formation while controlling pressure
US20030116315A1 (en) * 2001-04-24 2003-06-26 Wellington Scott Lee In situ thermal processing of a relatively permeable formation
US20030141067A1 (en) * 2001-04-24 2003-07-31 Rouffignac Eric Pierre De In situ thermal processing of an oil shale formation to increase permeability of the formation
US20030098149A1 (en) * 2001-04-24 2003-05-29 Wellington Scott Lee In situ thermal recovery from a relatively permeable formation using gas to increase mobility
US6991032B2 (en) 2001-04-24 2006-01-31 Shell Oil Company In situ thermal processing of an oil shale formation using a pattern of heat sources
US20030141066A1 (en) * 2001-04-24 2003-07-31 Karanikas John Michael In situ thermal processing of an oil shale formation while inhibiting coking
US6991033B2 (en) 2001-04-24 2006-01-31 Shell Oil Company In situ thermal processing while controlling pressure in an oil shale formation
US20030098605A1 (en) * 2001-04-24 2003-05-29 Vinegar Harold J. In situ thermal recovery from a relatively permeable formation
US6991036B2 (en) 2001-04-24 2006-01-31 Shell Oil Company Thermal processing of a relatively permeable formation
US20030136559A1 (en) * 2001-04-24 2003-07-24 Wellington Scott Lee In situ thermal processing while controlling pressure in an oil shale formation
US20030136558A1 (en) * 2001-04-24 2003-07-24 Wellington Scott Lee In situ thermal processing of an oil shale formation to produce a desired product
US20030131993A1 (en) * 2001-04-24 2003-07-17 Etuan Zhang In situ thermal processing of an oil shale formation with a selected property
US6994169B2 (en) 2001-04-24 2006-02-07 Shell Oil Company In situ thermal processing of an oil shale formation with a selected property
US20030131996A1 (en) * 2001-04-24 2003-07-17 Vinegar Harold J. In situ thermal processing of an oil shale formation having permeable and impermeable sections
US6997518B2 (en) 2001-04-24 2006-02-14 Shell Oil Company In situ thermal processing and solution mining of an oil shale formation
US7004251B2 (en) 2001-04-24 2006-02-28 Shell Oil Company In situ thermal processing and remediation of an oil shale formation
US7004247B2 (en) 2001-04-24 2006-02-28 Shell Oil Company Conductor-in-conduit heat sources for in situ thermal processing of an oil shale formation
US20030131995A1 (en) * 2001-04-24 2003-07-17 De Rouffignac Eric Pierre In situ thermal processing of a relatively impermeable formation to increase permeability of the formation
US20030164239A1 (en) * 2001-04-24 2003-09-04 Wellington Scott Lee In situ thermal processing of an oil shale formation in a reducing environment
US20030102126A1 (en) * 2001-04-24 2003-06-05 Sumnu-Dindoruk Meliha Deniz In situ thermal recovery from a relatively permeable formation with controlled production rate
US6981548B2 (en) 2001-04-24 2006-01-03 Shell Oil Company In situ thermal recovery from a relatively permeable formation
US20040211554A1 (en) * 2001-04-24 2004-10-28 Vinegar Harold J. Heat sources with conductive material for in situ thermal processing of an oil shale formation
US7040399B2 (en) 2001-04-24 2006-05-09 Shell Oil Company In situ thermal processing of an oil shale formation using a controlled heating rate
US7040400B2 (en) 2001-04-24 2006-05-09 Shell Oil Company In situ thermal processing of a relatively impermeable formation using an open wellbore
US7040398B2 (en) 2001-04-24 2006-05-09 Shell Oil Company In situ thermal processing of a relatively permeable formation in a reducing environment
US7051811B2 (en) 2001-04-24 2006-05-30 Shell Oil Company In situ thermal processing through an open wellbore in an oil shale formation
US7051807B2 (en) 2001-04-24 2006-05-30 Shell Oil Company In situ thermal recovery from a relatively permeable formation with quality control
US7066254B2 (en) 2001-04-24 2006-06-27 Shell Oil Company In situ thermal processing of a tar sands formation
US7055600B2 (en) 2001-04-24 2006-06-06 Shell Oil Company In situ thermal recovery from a relatively permeable formation with controlled production rate
US6877555B2 (en) 2001-04-24 2005-04-12 Shell Oil Company In situ thermal processing of an oil shale formation while inhibiting coking
US20030173085A1 (en) * 2001-10-24 2003-09-18 Vinegar Harold J. Upgrading and mining of coal
US7090013B2 (en) 2001-10-24 2006-08-15 Shell Oil Company In situ thermal processing of a hydrocarbon containing formation to produce heated fluids
US7128153B2 (en) 2001-10-24 2006-10-31 Shell Oil Company Treatment of a hydrocarbon containing formation after heating
US7077198B2 (en) 2001-10-24 2006-07-18 Shell Oil Company In situ recovery from a hydrocarbon containing formation using barriers
US20040040715A1 (en) * 2001-10-24 2004-03-04 Wellington Scott Lee In situ production of a blending agent from a hydrocarbon containing formation
US7063145B2 (en) 2001-10-24 2006-06-20 Shell Oil Company Methods and systems for heating a hydrocarbon containing formation in situ with an opening contacting the earth's surface at two locations
US7086465B2 (en) 2001-10-24 2006-08-08 Shell Oil Company In situ production of a blending agent from a hydrocarbon containing formation
US7077199B2 (en) 2001-10-24 2006-07-18 Shell Oil Company In situ thermal processing of an oil reservoir formation
US6991045B2 (en) 2001-10-24 2006-01-31 Shell Oil Company Forming openings in a hydrocarbon containing formation using magnetic tracking
US7165615B2 (en) 2001-10-24 2007-01-23 Shell Oil Company In situ recovery from a hydrocarbon containing formation using conductor-in-conduit heat sources with an electrically conductive material in the overburden
US6969123B2 (en) 2001-10-24 2005-11-29 Shell Oil Company Upgrading and mining of coal
US7100994B2 (en) 2001-10-24 2006-09-05 Shell Oil Company Producing hydrocarbons and non-hydrocarbon containing materials when treating a hydrocarbon containing formation
US7104319B2 (en) 2001-10-24 2006-09-12 Shell Oil Company In situ thermal processing of a heavy oil diatomite formation
US7114566B2 (en) 2001-10-24 2006-10-03 Shell Oil Company In situ thermal processing of a hydrocarbon containing formation using a natural distributed combustor
US20030201098A1 (en) * 2001-10-24 2003-10-30 Karanikas John Michael In situ recovery from a hydrocarbon containing formation using one or more simulations
US20050092483A1 (en) * 2001-10-24 2005-05-05 Vinegar Harold J. In situ thermal processing of a hydrocarbon containing formation using a natural distributed combustor
US7156176B2 (en) 2001-10-24 2007-01-02 Shell Oil Company Installation and use of removable heaters in a hydrocarbon containing formation
US7051808B1 (en) 2001-10-24 2006-05-30 Shell Oil Company Seismic monitoring of in situ conversion in a hydrocarbon containing formation
US7461691B2 (en) 2001-10-24 2008-12-09 Shell Oil Company In situ recovery from a hydrocarbon containing formation
US8627887B2 (en) 2001-10-24 2014-01-14 Shell Oil Company In situ recovery from a hydrocarbon containing formation
US20030173081A1 (en) * 2001-10-24 2003-09-18 Vinegar Harold J. In situ thermal processing of an oil reservoir formation
US20030196810A1 (en) * 2001-10-24 2003-10-23 Vinegar Harold J. Treatment of a hydrocarbon containing formation after heating
US7066257B2 (en) 2001-10-24 2006-06-27 Shell Oil Company In situ recovery from lean and rich zones in a hydrocarbon containing formation
US6932155B2 (en) 2001-10-24 2005-08-23 Shell Oil Company In situ thermal processing of a hydrocarbon containing formation via backproducing through a heater well
US7219734B2 (en) 2002-10-24 2007-05-22 Shell Oil Company Inhibiting wellbore deformation during in situ thermal processing of a hydrocarbon containing formation
US8238730B2 (en) 2002-10-24 2012-08-07 Shell Oil Company High voltage temperature limited heaters
US8224163B2 (en) 2002-10-24 2012-07-17 Shell Oil Company Variable frequency temperature limited heaters
US8224164B2 (en) 2002-10-24 2012-07-17 Shell Oil Company Insulated conductor temperature limited heaters
US7073578B2 (en) 2002-10-24 2006-07-11 Shell Oil Company Staged and/or patterned heating during in situ thermal processing of a hydrocarbon containing formation
US7121341B2 (en) 2002-10-24 2006-10-17 Shell Oil Company Conductor-in-conduit temperature limited heaters
US8579031B2 (en) 2003-04-24 2013-11-12 Shell Oil Company Thermal processes for subsurface formations
US7942203B2 (en) 2003-04-24 2011-05-17 Shell Oil Company Thermal processes for subsurface formations
US7121342B2 (en) 2003-04-24 2006-10-17 Shell Oil Company Thermal processes for subsurface formations
US7360588B2 (en) 2003-04-24 2008-04-22 Shell Oil Company Thermal processes for subsurface formations
US7353872B2 (en) 2004-04-23 2008-04-08 Shell Oil Company Start-up of temperature limited heaters using direct current (DC)
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
US7357180B2 (en) 2004-04-23 2008-04-15 Shell Oil Company Inhibiting effects of sloughing in wellbores
US7320364B2 (en) 2004-04-23 2008-01-22 Shell Oil Company Inhibiting reflux in a heated well of an in situ conversion system
US20050269091A1 (en) * 2004-04-23 2005-12-08 Guillermo Pastor-Sanz Reducing viscosity of oil for production from a hydrocarbon containing formation
US7370704B2 (en) 2004-04-23 2008-05-13 Shell Oil Company Triaxial temperature limited heater
US7510000B2 (en) 2004-04-23 2009-03-31 Shell Oil Company Reducing viscosity of oil for production from a hydrocarbon containing formation
US7383877B2 (en) 2004-04-23 2008-06-10 Shell Oil Company 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
US7424915B2 (en) 2004-04-23 2008-09-16 Shell Oil Company Vacuum pumping of conductor-in-conduit heaters
US8355623B2 (en) 2004-04-23 2013-01-15 Shell Oil Company Temperature limited heaters with high power factors
US8224165B2 (en) 2005-04-22 2012-07-17 Shell Oil Company Temperature limited heater utilizing non-ferromagnetic conductor
US20070108200A1 (en) * 2005-04-22 2007-05-17 Mckinzie Billy J Ii Low temperature barrier wellbores formed using water flushing
US7575052B2 (en) 2005-04-22 2009-08-18 Shell Oil Company In situ conversion process utilizing a closed loop heating system
US8070840B2 (en) 2005-04-22 2011-12-06 Shell Oil Company Treatment of gas 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
US8233782B2 (en) 2005-04-22 2012-07-31 Shell Oil Company Grouped exposed metal heaters
US7546873B2 (en) 2005-04-22 2009-06-16 Shell Oil Company Low temperature barriers for use with in situ processes
US8027571B2 (en) 2005-04-22 2011-09-27 Shell Oil Company In situ conversion process systems utilizing wellbores in at least two regions of a formation
US7527094B2 (en) 2005-04-22 2009-05-05 Shell Oil Company Double barrier system for an in situ conversion process
US7575053B2 (en) 2005-04-22 2009-08-18 Shell Oil Company Low temperature monitoring system for subsurface barriers
US20070045265A1 (en) * 2005-04-22 2007-03-01 Mckinzie Billy J Ii Low temperature barriers with heat interceptor wells for in situ processes
US7986869B2 (en) 2005-04-22 2011-07-26 Shell Oil Company Varying properties along lengths of temperature limited heaters
US20070137856A1 (en) * 2005-04-22 2007-06-21 Mckinzie Billy J Double barrier system for an in situ conversion process
US7435037B2 (en) 2005-04-22 2008-10-14 Shell Oil Company Low temperature barriers with heat interceptor wells for in situ processes
US7942197B2 (en) 2005-04-22 2011-05-17 Shell Oil Company Methods and systems for producing fluid from an in situ conversion process
US7860377B2 (en) 2005-04-22 2010-12-28 Shell Oil Company Subsurface connection methods for subsurface heaters
US7500528B2 (en) 2005-04-22 2009-03-10 Shell Oil Company Low temperature barrier wellbores formed using water flushing
US7831134B2 (en) 2005-04-22 2010-11-09 Shell Oil Company Grouped exposed metal heaters
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
US20070221377A1 (en) * 2005-10-24 2007-09-27 Vinegar Harold J Solution mining systems and methods for treating hydrocarbon containing formations
US20080107577A1 (en) * 2005-10-24 2008-05-08 Vinegar Harold J Varying heating in dawsonite zones in hydrocarbon containing formations
US8151880B2 (en) 2005-10-24 2012-04-10 Shell Oil Company Methods of making transportation fuel
US20070131427A1 (en) * 2005-10-24 2007-06-14 Ruijian Li Systems and methods for producing hydrocarbons from tar sands formations
US20070131419A1 (en) * 2005-10-24 2007-06-14 Maria Roes Augustinus W Methods of producing alkylated hydrocarbons from an in situ heat treatment process liquid
US20070095536A1 (en) * 2005-10-24 2007-05-03 Vinegar Harold J Cogeneration systems and processes for treating hydrocarbon containing formations
US8606091B2 (en) 2005-10-24 2013-12-10 Shell Oil Company Subsurface heaters with low sulfidation rates
US20070131420A1 (en) * 2005-10-24 2007-06-14 Weijian Mo Methods of cracking a crude product to produce additional crude products
US20070127897A1 (en) * 2005-10-24 2007-06-07 John Randy C Subsurface heaters with low sulfidation rates
US20070125533A1 (en) * 2005-10-24 2007-06-07 Minderhoud Johannes K Methods of hydrotreating a liquid stream to remove clogging compounds
US7559368B2 (en) 2005-10-24 2009-07-14 Shell Oil Company Solution mining systems and methods for treating hydrocarbon containing formations
US7597147B2 (en) 2006-04-21 2009-10-06 Shell Oil Company Temperature limited heaters using phase transformation of ferromagnetic material
US7866385B2 (en) 2006-04-21 2011-01-11 Shell Oil Company Power systems utilizing the heat of produced formation fluid
US20080173450A1 (en) * 2006-04-21 2008-07-24 Bernard Goldberg Time sequenced heating of multiple layers in a hydrocarbon containing formation
US7533719B2 (en) 2006-04-21 2009-05-19 Shell Oil Company Wellhead with non-ferromagnetic materials
US20080035348A1 (en) * 2006-04-21 2008-02-14 Vitek John M Temperature limited heaters using phase transformation of ferromagnetic material
US20080035705A1 (en) * 2006-04-21 2008-02-14 Menotti James L Welding shield for coupling heaters
US7793722B2 (en) 2006-04-21 2010-09-14 Shell Oil Company Non-ferromagnetic overburden casing
US7785427B2 (en) 2006-04-21 2010-08-31 Shell Oil Company High strength alloys
US20080174115A1 (en) * 2006-04-21 2008-07-24 Gene Richard Lambirth Power systems utilizing the heat of produced formation fluid
US20080173449A1 (en) * 2006-04-21 2008-07-24 Thomas David Fowler Sour gas injection for use with in situ heat treatment
US20080035346A1 (en) * 2006-04-21 2008-02-14 Vijay Nair Methods of producing transportation fuel
US8857506B2 (en) 2006-04-21 2014-10-14 Shell Oil Company Alternate energy source usage methods for in situ heat treatment processes
US20080173442A1 (en) * 2006-04-21 2008-07-24 Vinegar Harold J Sulfur barrier for use with in situ processes for treating formations
US7912358B2 (en) 2006-04-21 2011-03-22 Shell Oil Company Alternate energy source usage for in situ heat treatment processes
US8192682B2 (en) 2006-04-21 2012-06-05 Shell Oil Company High strength alloys
US20080173444A1 (en) * 2006-04-21 2008-07-24 Francis Marion Stone Alternate energy source usage for in situ heat treatment processes
US7683296B2 (en) 2006-04-21 2010-03-23 Shell Oil Company Adjusting alloy compositions for selected properties in temperature limited heaters
US7673786B2 (en) 2006-04-21 2010-03-09 Shell Oil Company Welding shield for coupling heaters
US7635023B2 (en) 2006-04-21 2009-12-22 Shell Oil Company Time sequenced heating of multiple layers in a hydrocarbon containing formation
US20080038144A1 (en) * 2006-04-21 2008-02-14 Maziasz Phillip J High strength alloys
US8083813B2 (en) 2006-04-21 2011-12-27 Shell Oil Company Methods of producing transportation fuel
US7631689B2 (en) 2006-04-21 2009-12-15 Shell Oil Company Sulfur barrier for use with in situ processes for treating formations
US7703513B2 (en) 2006-10-20 2010-04-27 Shell Oil Company Wax barrier for use with in situ processes for treating formations
US7644765B2 (en) 2006-10-20 2010-01-12 Shell Oil Company Heating tar sands formations while controlling pressure
US20080135253A1 (en) * 2006-10-20 2008-06-12 Vinegar Harold J Treating tar sands formations with karsted zones
US8191630B2 (en) 2006-10-20 2012-06-05 Shell Oil Company Creating fluid injectivity in tar sands formations
US20080277113A1 (en) * 2006-10-20 2008-11-13 George Leo Stegemeier Heating tar sands formations while controlling pressure
US7673681B2 (en) 2006-10-20 2010-03-09 Shell Oil Company Treating tar sands formations with karsted zones
US20090014181A1 (en) * 2006-10-20 2009-01-15 Vinegar Harold J 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
US7677310B2 (en) 2006-10-20 2010-03-16 Shell Oil Company Creating and maintaining a gas cap in tar sands formations
US7681647B2 (en) 2006-10-20 2010-03-23 Shell Oil Company Method of producing drive fluid in situ in tar sands formations
US20080142217A1 (en) * 2006-10-20 2008-06-19 Roelof Pieterson Using geothermal energy to heat a portion of a formation for an in situ heat treatment process
US20080185147A1 (en) * 2006-10-20 2008-08-07 Vinegar Harold J Wax barrier for use with in situ processes for treating formations
US20080135254A1 (en) * 2006-10-20 2008-06-12 Vinegar Harold J In situ heat treatment process utilizing a closed loop heating system
US20080128134A1 (en) * 2006-10-20 2008-06-05 Ramesh Raju Mudunuri Producing drive fluid in situ in tar sands formations
US7635024B2 (en) 2006-10-20 2009-12-22 Shell Oil Company Heating tar sands formations to visbreaking temperatures
US20080142216A1 (en) * 2006-10-20 2008-06-19 Vinegar Harold J Treating tar sands formations with dolomite
US20080135244A1 (en) * 2006-10-20 2008-06-12 David Scott Miller Heating hydrocarbon containing formations in a line drive staged process
US20080217004A1 (en) * 2006-10-20 2008-09-11 De Rouffignac Eric Pierre Heating hydrocarbon containing formations in a checkerboard pattern staged process
US7845411B2 (en) 2006-10-20 2010-12-07 Shell Oil Company In situ heat treatment process utilizing a closed loop heating system
US7717171B2 (en) 2006-10-20 2010-05-18 Shell Oil Company Moving hydrocarbons through portions of tar sands formations with a fluid
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
US7730946B2 (en) 2006-10-20 2010-06-08 Shell Oil Company Treating tar sands formations with dolomite
US20080217015A1 (en) * 2006-10-20 2008-09-11 Vinegar Harold J 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
US20090014180A1 (en) * 2006-10-20 2009-01-15 George Leo Stegemeier Moving hydrocarbons through portions of tar sands formations with a fluid
US20080217003A1 (en) * 2006-10-20 2008-09-11 Myron Ira Kuhlman Gas injection to inhibit migration during an in situ heat treatment process
US7841401B2 (en) 2006-10-20 2010-11-30 Shell Oil Company Gas injection to inhibit migration during an in situ heat treatment process
US7798220B2 (en) 2007-04-20 2010-09-21 Shell Oil Company In situ heat treatment of a tar sands formation after drive process treatment
US7931086B2 (en) 2007-04-20 2011-04-26 Shell Oil Company Heating systems for heating subsurface formations
US7841425B2 (en) 2007-04-20 2010-11-30 Shell Oil Company Drilling subsurface wellbores with cutting structures
US7841408B2 (en) 2007-04-20 2010-11-30 Shell Oil Company In situ heat treatment from multiple layers of a tar sands formation
US9181780B2 (en) 2007-04-20 2015-11-10 Shell Oil Company Controlling and assessing pressure conditions during treatment of tar sands formations
US7849922B2 (en) 2007-04-20 2010-12-14 Shell Oil Company In situ recovery from residually heated sections in a hydrocarbon containing formation
US20090071652A1 (en) * 2007-04-20 2009-03-19 Vinegar Harold J In situ heat treatment from multiple layers of a tar sands formation
US20090078461A1 (en) * 2007-04-20 2009-03-26 Arthur James Mansure Drilling subsurface wellbores with cutting structures
US8327681B2 (en) 2007-04-20 2012-12-11 Shell Oil Company Wellbore manufacturing processes for in situ heat treatment processes
US20090126929A1 (en) * 2007-04-20 2009-05-21 Vinegar Harold J Treating nahcolite containing formations and saline zones
US8791396B2 (en) 2007-04-20 2014-07-29 Shell Oil Company Floating insulated conductors for heating subsurface formations
US20090095479A1 (en) * 2007-04-20 2009-04-16 John Michael Karanikas Production from multiple zones 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
US7832484B2 (en) 2007-04-20 2010-11-16 Shell Oil Company Molten salt as a heat transfer fluid for heating a subsurface formation
US7950453B2 (en) 2007-04-20 2011-05-31 Shell Oil Company Downhole burner systems and methods for heating subsurface formations
US20090084547A1 (en) * 2007-04-20 2009-04-02 Walter Farman Farmayan Downhole burner systems and methods for heating subsurface formations
US8381815B2 (en) 2007-04-20 2013-02-26 Shell Oil Company Production from multiple zones of a tar sands formation
US20090090509A1 (en) * 2007-04-20 2009-04-09 Vinegar Harold J In situ recovery from residually heated sections in a hydrocarbon containing formation
US8042610B2 (en) 2007-04-20 2011-10-25 Shell Oil Company Parallel heater system for subsurface formations
US20090095480A1 (en) * 2007-04-20 2009-04-16 Vinegar Harold J In situ heat treatment of a tar sands formation after drive process treatment
US20090095476A1 (en) * 2007-04-20 2009-04-16 Scott Vinh Nguyen Molten salt as a heat transfer fluid for heating a subsurface formation
US8459359B2 (en) 2007-04-20 2013-06-11 Shell Oil Company Treating nahcolite containing formations and saline zones
US20090095477A1 (en) * 2007-04-20 2009-04-16 Scott Vinh Nguyen Heating systems for heating subsurface formations
US8113272B2 (en) 2007-10-19 2012-02-14 Shell Oil Company Three-phase heaters with common overburden sections for heating subsurface formations
US8146661B2 (en) 2007-10-19 2012-04-03 Shell Oil Company Cryogenic treatment of gas
US8536497B2 (en) 2007-10-19 2013-09-17 Shell Oil Company Methods for forming long subsurface heaters
US8162059B2 (en) 2007-10-19 2012-04-24 Shell Oil Company Induction heaters used to heat subsurface formations
US8146669B2 (en) 2007-10-19 2012-04-03 Shell Oil Company Multi-step heater deployment in a subsurface formation
US8272455B2 (en) 2007-10-19 2012-09-25 Shell Oil Company Methods for forming wellbores in heated formations
US8011451B2 (en) 2007-10-19 2011-09-06 Shell Oil Company Ranging methods for developing wellbores in subsurface formations
US7866386B2 (en) 2007-10-19 2011-01-11 Shell Oil Company In situ oxidation of subsurface formations
US20090200025A1 (en) * 2007-10-19 2009-08-13 Jose Luis Bravo High temperature methods for forming oxidizer fuel
US8196658B2 (en) 2007-10-19 2012-06-12 Shell Oil Company Irregular spacing of heat sources for treating hydrocarbon containing formations
US20090200854A1 (en) * 2007-10-19 2009-08-13 Vinegar Harold J Solution mining and in situ treatment of nahcolite beds
US20090200031A1 (en) * 2007-10-19 2009-08-13 David Scott Miller Irregular spacing of heat sources for treating hydrocarbon containing formations
US20090194282A1 (en) * 2007-10-19 2009-08-06 Gary Lee Beer In situ oxidation of subsurface formations
US7866388B2 (en) 2007-10-19 2011-01-11 Shell Oil Company High temperature methods for forming oxidizer fuel
US20090194329A1 (en) * 2007-10-19 2009-08-06 Rosalvina Ramona Guimerans Methods for forming wellbores in heated formations
US20090194269A1 (en) * 2007-10-19 2009-08-06 Vinegar Harold J Three-phase heaters with common overburden sections for heating subsurface formations
US20090194524A1 (en) * 2007-10-19 2009-08-06 Dong Sub Kim Methods for forming long subsurface heaters
US20090189617A1 (en) * 2007-10-19 2009-07-30 David Burns Continuous subsurface heater temperature measurement
US8240774B2 (en) 2007-10-19 2012-08-14 Shell Oil Company Solution mining and in situ treatment of nahcolite beds
US8276661B2 (en) 2007-10-19 2012-10-02 Shell Oil Company Heating subsurface formations by oxidizing fuel on a fuel carrier
US8636323B2 (en) 2008-04-18 2014-01-28 Shell Oil Company Mines and tunnels for use in treating subsurface hydrocarbon containing formations
US8172335B2 (en) 2008-04-18 2012-05-08 Shell Oil Company Electrical current flow between tunnels for use in heating 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
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
US20090272535A1 (en) * 2008-04-18 2009-11-05 David Booth Burns Using tunnels for treating subsurface hydrocarbon containing formations
US20090272533A1 (en) * 2008-04-18 2009-11-05 David Booth Burns Heated fluid flow in mines and tunnels used in heating subsurface hydrocarbon containing formations
US20090272578A1 (en) * 2008-04-18 2009-11-05 Macdonald Duncan Charles Dual motor systems and non-rotating sensors for use in developing wellbores in subsurface 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
US20090260823A1 (en) * 2008-04-18 2009-10-22 Robert George Prince-Wright Mines and tunnels for use in treating subsurface hydrocarbon containing formations
US20090260824A1 (en) * 2008-04-18 2009-10-22 David Booth Burns Hydrocarbon production from mines and tunnels used in treating 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
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
US8162405B2 (en) 2008-04-18 2012-04-24 Shell Oil Company Using tunnels for treating subsurface hydrocarbon containing formations
US8353347B2 (en) 2008-10-13 2013-01-15 Shell Oil Company Deployment of insulated conductors for treating subsurface formations
US20100096137A1 (en) * 2008-10-13 2010-04-22 Scott Vinh Nguyen Circulated heated transfer fluid heating of subsurface hydrocarbon formations
US20100108379A1 (en) * 2008-10-13 2010-05-06 David Alston Edbury Systems and methods of forming subsurface wellbores
US8881806B2 (en) 2008-10-13 2014-11-11 Shell Oil Company Systems and methods for treating a subsurface formation with electrical conductors
US9022118B2 (en) 2008-10-13 2015-05-05 Shell Oil Company Double insulated heaters for treating 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
US8281861B2 (en) 2008-10-13 2012-10-09 Shell Oil Company Circulated heated transfer fluid heating of subsurface hydrocarbon formations
US8256512B2 (en) 2008-10-13 2012-09-04 Shell Oil Company Movable heaters for treating subsurface hydrocarbon containing formations
US20100089584A1 (en) * 2008-10-13 2010-04-15 David Booth Burns Double insulated heaters for treating subsurface formations
US8261832B2 (en) 2008-10-13 2012-09-11 Shell Oil Company Heating subsurface formations with fluids
US20100089586A1 (en) * 2008-10-13 2010-04-15 John Andrew Stanecki Movable heaters for treating subsurface hydrocarbon containing formations
US9051829B2 (en) 2008-10-13 2015-06-09 Shell Oil Company Perforated electrical 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
US20100108310A1 (en) * 2008-10-13 2010-05-06 Thomas David Fowler Offset barrier wells in subsurface formations
US9129728B2 (en) 2008-10-13 2015-09-08 Shell Oil Company Systems and methods of forming subsurface wellbores
US8267170B2 (en) 2008-10-13 2012-09-18 Shell Oil Company Offset barrier wells in subsurface formations
US20100101784A1 (en) * 2008-10-13 2010-04-29 Vinegar Harold J Controlling hydrogen pressure in self-regulating nuclear reactors used to treat a subsurface formation
US20100101783A1 (en) * 2008-10-13 2010-04-29 Vinegar Harold J Using self-regulating nuclear reactors in treating a subsurface formation
US8448707B2 (en) 2009-04-10 2013-05-28 Shell Oil Company Non-conducting heater casings
US8327932B2 (en) 2009-04-10 2012-12-11 Shell Oil Company Recovering energy from a subsurface formation
US8851170B2 (en) 2009-04-10 2014-10-07 Shell Oil Company Heater assisted fluid treatment of a subsurface formation
US8434555B2 (en) 2009-04-10 2013-05-07 Shell Oil Company Irregular pattern treatment of a subsurface formation
US8701769B2 (en) 2010-04-09 2014-04-22 Shell Oil Company Methods for treating hydrocarbon formations based on geology
US9127538B2 (en) 2010-04-09 2015-09-08 Shell Oil Company Methodologies for treatment of hydrocarbon formations using staged pyrolyzation
US9022109B2 (en) 2010-04-09 2015-05-05 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
US9033042B2 (en) 2010-04-09 2015-05-19 Shell Oil Company Forming bitumen barriers 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
US9127523B2 (en) 2010-04-09 2015-09-08 Shell Oil Company Barrier methods for use in subsurface hydrocarbon formations
US8631866B2 (en) 2010-04-09 2014-01-21 Shell Oil Company Leak detection in circulated fluid systems for heating subsurface formations
US8739874B2 (en) 2010-04-09 2014-06-03 Shell Oil Company Methods for heating with slots in hydrocarbon formations
US8701768B2 (en) 2010-04-09 2014-04-22 Shell Oil Company Methods for treating hydrocarbon formations
US9399905B2 (en) 2010-04-09 2016-07-26 Shell Oil Company Leak detection in circulated fluid systems for heating subsurface formations
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
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
US3110345A (en) Low temperature reverse combustion process
US3097690A (en) Process for heating a subsurface formation
US3007521A (en) Recovery of oil by in situ combustion
US2825408A (en) Oil recovery by subsurface thermal processing
US2793696A (en) Oil recovery by underground combustion
US2734579A (en) Production from bituminous sands
US3209825A (en) Low temperature in-situ combustion
US3106244A (en) Process for producing oil shale in situ by electrocarbonization
US3150715A (en) Oil recovery by in situ combustion with water injection
US2994376A (en) In situ combustion process
US3013609A (en) Method for producing hydrocarbons in an in situ combustion operation
US3542131A (en) Method of recovering hydrocarbons from oil shale
US3116792A (en) In situ combustion process
US3456721A (en) Downhole-burner apparatus
US3138203A (en) Method of underground burning
US3055423A (en) Controlling selective plugging of carbonaceous strata for controlled production of thermal drive
US3490529A (en) Production of oil from a nuclear chimney in an oil shale by in situ combustion
US2946382A (en) Process for recovering hydrocarbons from underground formations
US4691773A (en) Insitu wet combustion process for recovery of heavy oils
US3406755A (en) Forward in situ combustion method for reocvering hydrocarbons with production well cooling
US3362471A (en) In situ retorting of oil shale by transient state fluid flows
US3024841A (en) Method of oil recovery by in situ combustion
US3010707A (en) Recovery of resins and hydrocarbons from resinous type coals
US4109718A (en) Method of breaking shale oil-water emulsion
US2917296A (en) Recovery of hydrocarbon from oil shale adjoining a permeable oilbearing stratum