US3244231A - Method for catalytically heating oil bearing formations - Google Patents

Method for catalytically heating oil bearing formations Download PDF

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US3244231A
US3244231A US27166463A US3244231A US 3244231 A US3244231 A US 3244231A US 27166463 A US27166463 A US 27166463A US 3244231 A US3244231 A US 3244231A
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formation
catalyst
well
oil
tubing
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Grekel Howard
Karol L Hujsak
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Pan American Petroleum Corp
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Pan American Petroleum Corp
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    • EFIXED CONSTRUCTIONS
    • E21EARTH DRILLING; MINING
    • E21BEARTH DRILLING, e.g. DEEP DRILLING; OBTAINING OIL, GAS, WATER, SOLUBLE OR MELTABLE MATERIALS OR A SLURRY OF MINERALS FROM WELLS
    • E21B36/00Heating, cooling, insulating arrangements for boreholes or wells, e.g. for use in permafrost zones
    • E21B36/02Heating, cooling, insulating arrangements for boreholes or wells, e.g. for use in permafrost zones using burners

Description

A ril 5, 1966 H. GREKEL vEma. 3,244,231

I METHOD FOR CATALYTICALLY HEATING OIL BEARING FORMATIONS Filed April 9, 1963 4 Sheets-Sheet 1 HOWARD GREKEL KAROL L. HUJSAK INVENTORS. FIG-1 BY 2 ATTORNEY.

P 1955 H. GREKEL ETAL 3,244,331

METHOD FOR CATALYTIC-5L1 HEATING OIL BEARING FORMATIONS Filed April 9, 1963 4 SheetS Sheat 2 HOWARD GREKEL KAROL L. HUJSAK INVENTORS.

BY M4 Map 1.7

ATTORNEY.

9 1966 H. GREKEL ETAL 3,244,231

METHOD FOR CATALYTIOALLY HEATING OIL BEARING FORMATIONS Filed April 9, 1963 4 Sheets-Sheet s I 74 62\ ,r64 -f 68" 5 FlG.-9

HOWARD GREKEL KAROL L. HUJSAK INVENTORS.

ATTORNEY.

April 5, 1-966 H. GREKEL ETAL 3,244,231

METHOD FOR CATALYTICALLY HEATING OIL BEARING FORMATIONS Filed April 9, 1963 4 Sheets-Sheet 4 MOL PER CENT METHANOL IN FEED IOOC TEMPERATURE RISE 20 3O 4O 5O 6O 7O 8O SCF AlR/SCF METHANOL VAPOR Bi -"ll HOWAR D GREKEL KAROL L. HUJSAK INVENTORS.

ATTORNEY.

United States Patent Ofiice 3,244,231 Patented Apr. 5, 1966 METHOD FOR CATALYTICALLY HEATING OIL BEARING FGRMATIONS Howard Greirel and Karol L. Hujsak, Tulsa, Okla, as-

signors to Pan American Petroleum Corporation, Tulsa, Okla, a corporation of Delaware Filed Apr. 9, 1963, Ser. No. 271,664 13 Claims. (Cl. 166-38) The present invention relates to a method for heating and stimulating oil wells. More particularly, it is concerned with a method suitable for heating oil bearing or similar formations to a temperature sufficient either for stimulating the flow of oil therefrom or for igniting such formation to recover oil by means of combustion.

Briefly, our invention contemplates supplying heat to an oil bearing zone through the use of a catalytic heater especially adapted for the generation of heat by catalytic oxidation of any of a number of different fuels.

Many methods have been employed in the prior art for heating oil wells, e.g., by electrical means, by injecting heat transfer agents into the well such as steam, hot oil, etc., and by burning natural gas in the well bore. Considerable difficulty has been encountered in the application of electric well heating owing to the highly corrosive nature of oil field brine, sulfur compounds, and other components of the fluids produced through the well bore. These fluids penetrate the innermost parts of the well heater, and even traces of moisture cause short-circuiting of the apparatus necessitating shutdown, removal and repair. These difiiculties materially reduce the operating efliciency of such heating processes. Well bore liquids also penetrate and permeate the customary insulating materials rendering them practically useless. These problems are peculiar to the well heating art and are not generally encountered in other applications of electrical heating.

One of the principal drawbacks of the gas or liquid fueled heaters is that it is extremely difficult to avoid damage to the casing and any well equipment present in the area where heat is being applied. This is due to the fact that the temperature at which heaters of this kind operate cannot be maintained at levels which such equipment can withstand. One of the difficulties with electrical heaters is their tendency to short out owing to hot spots developing through poor heat exchange, generally resulting from coke formation on the surface. With increasing thickness of the coke layer on the exterior of the heater, the temperature tends to build up until it exceeds the melting point of the heating elements causing the latter to fail.

' It is another object of our invention to provide a method for heating oil bearing zones that permits easy and effective temperature control at reasonable operating costs. It is a further object of our invention to provide a method for stimulating the flow of oil from an underground deposit thereof by the use of heat without the formation of coke in objectionable amounts.

In the accompanying drawings a number of embodiments of our invention are illustrated:

FIGURE 1 shows an over-all, partly sectional, view of one embodiment of the apparatus used in accordance with our invention to heat an oil bearing zone by means of catalytic oxidation.

FIGURE 2 is a modification of-the design shown in FIGURE 1 in which the efliuent from the catalyst bed travels back up the annulus formed by the concentric arrangement of tubing thereby allowing further control of the heater skin temperature which, in turn, aids materially in preventing excessive deposition of coke on the unit.

FIGURE 3 is a detailed design, in section, of a cata-' lytic bottom hole heater or igniter which can be operated on a wire line and hung from tubing. The base of the heater is composed of a heavy stainless steel screen to permit passage of gases while still supporting the catalyst bed.

FIGURE 4 is a plan view of the top of heater shown in FIGURE 3, having suitable cross-pieces for attachment to the wire line.

FIGURE 5 is an elevational view, partly in section, showing an adaptation of our invention wherein the heater is in operation while the well is being pumped.

FIGURE 6 is a detailed design of one form of catalytice bottom hole heater mounted on tubing as contemplated by our invention.

FIGURE 7 is a cross-section of FIGURE 6 taken along line 6-6, showing in somewhat more detail the structure of the apparatus displayed in FIGURE 6.

FIGURE 8 is still another variation of the catalytic bottom hole heater mountable on tubing, as contemplated by our invention.

FIGURE 9 is a modification of the upper portion of the heater design shown in FIGURES 6 and 8.

FIGURE 10 is another sectional view illustrating a design of our invention wherein heating of the formation and simultaneous pumping of the well are effected with the use of a single string of tubing.

FIGURE 11 is a plot showing the volume ratio of air to fuel (methanol in this case) required to produce a given gas effluent temperature from the catalyst bed; it also shows the concentration of methanol in the feed in terms of mole percent to generate a given temperature.

Referring now to FIGURE 1, a protective casing 2 is shown extending from the earth's surface down to an oil-bearing zone 4 which communicates with the casing via perforations 8. Within casing 2 is a string of production tubing 10 which may extend above, below or substantially within the vertical distance covered by perforations 8. concentrically disposed in tubing 10 is a second tubing 12 which may or may not extend into the well to the depth of perforations 8. At the base of tubing 12 is a seating nipple 14 into which catalytic heater 16 is lowered on wire line 18 and seated. A fuel-air mixture having a composition outside the explosive limit and in proper proportions for generating gas effluent temperatures from heater 16 of from about 500 to about 1000 F. is introduced into tubing 12 via valved flow line 20. On contacting the catalyst in heater 16 with the aforesaid mixture, the oxidation of the fuel creates combustion products having a temperature within the above-stated range. The combustion products, including excess air, are produced either through casing or through the annulus between tubing 12 and tubing 16v and out line 22 along with the produced oil. When the combustion products are produced with the oil, the amount of air used is regulated such that there is no possibility of developing explosive mixtures or excessive temperatures if it reacts with the produced oil.

In the case where it is desired to heat formation 4 to ignition temperature, i.e., preferably of the order of 800 to 1000 F., prior to conducting a combustion process, production tubing 10 is omitted. Well fluids are forced back into the formation by means of gas pressure until they have dropped to a level in the well below perforations 8. The hot combustion gases are then directed into formation 4 via perforations 8, or casing 2 may be landed near the top of formation 4 in which case the hot gases from heater 16 are directed to the walls of the open hole extending into said formation. In this heating step the well head and valved line 22 is closed, of course, so that the hot gases are directed to all of the formation 4. This same procedure may be used where it is desired merely to heat up the formation within a radius of 10 to 15 feet, for example, from the well bore in order to stimulate the flow of oil. It will also be appreciated, of course, that thistechnique may be employed in open hole preparatory to combustion operations. It should be pointed out that in case it is found desirable to preheat the fuelair mixture in tubing 12, valved line 22 may be left open slightly. so that a small stream of hot oxidation products flows up the annulus, thereby furnishing heat to said mixture.

If;the aforesaid heating step is carried outfor the purpose of initiating a combustion process, heater 16, after the formation ignition temperature is reached, is removed from the well and the latter becomes either a producing or an injection well, depending on whether it is being used. in a reverse or forward combustion drive. If the well is. employed as a producer, oil is produced through line 22, and if it is used as an injection well, air is introduced into the formation via line 26.

In FIGURE 2, heater 16. may be either in the form as shown in FIGURES l or 3, i.e., all of the fuel-air mixture flows through only. a portion of the catalyst bed or said mixture may flow through the entire bed.

Where it is desired to employ a bottom hole heater for the purpose of preventing accumulation of paraffin at or near the face of the formation and in the tubing, an arrangement such as that shown in FIGURE may be used. In this case, tubing 24, carrying heater 26, is secured to well head 28;. Heater 26 is threadedly or otherwise removably mounted to tubing 24 at 30. The necessary fuel-air mixture is supplied to the heater via valved line 32. The structure of heater 26 is shown in further detail in FIGURES 6 and 7, in which an elongated cylindrical vessel 33, measuring usually to 20 feet in length and about 2 inches O.D., is filled with a suitable oxidation catalyst 34. The catalyst is supported at a level near the base. of the-heater by means of a stainless steel screen 36.. At the mouth of heater 26 fuel line 32 extends into vessel 33. for a short distance above thetop of catalyst 34. Line 32,is held in alignment with the mouth of vessel 33 by meansof metal seal 38. Tubes 40 fit snugly against the exterior of vessel 33 and place into communication the space below screen 36 with the open area just above seal 38 in tubing 24. The total cross-sectional area of tubes 4,0.sho u1d be large enough, in proportion to that of vessel 33, to avoid excessive pressure drop.

Production tubing 42 isequipped at the lower end with a check orstanding valve 44 which permits flow of oil from formation 4 into tubing 42 but prevents reverse flow. The. flow-of. oil through the system is maintained by the reciprocal motion ofpump 46 connected to sucker rod 48extending upwardly to the surface. through tubing 42 tosuitable, power means (not shown) located at the surface. O'il pumped from thewell in this fashion is removed-by means of flow line 50.

The heater shown in FIGURE 8 can be substituted for the, one illustrated in FIGURE 5, shown in moredetail inFIGURE6. The device in FIGURE 8 is somewhat simpler indesign andincludes an elongated metal case 52 ,holclinga bed of catalyst 34supported at the base by a grate or screen 54. Screen 54 is secured both to the interior of case 52 and to the base of tubing 32. A similar. tructure57 is placed at the top of the bed to prevent entrainment. of the catalyst with the fluids flowing upwardly into the annulus between tubing strings 24 and 5.6; The upper portion of case 52 is engaged to tubing 24 at threaded connection 30.

I In operation of anassembly such as that shown in FIG- URES, asuitable fuel-air mixture is forced down line 32 into contact with the catalyst as shown in the heater of FIGURES; Rapidoxidation of the hydrocarbon or oxyg enated organic compound in the feed occurs, generating temperatures of the order of from 400 to 800 or 1000 F; Thehot products of combustion flow through catalyst 3.4- down to the base-of the heater and then flow upwardly through tubes 40. Heat in these tubes, as well as in vessel 33, is extracted therefrom and transferred to surrounding well fluids which, in turn, release this heat to formation 4. After the heat has been largely removed from the gaseous products in tubes 4!), said products flow, as indicated, into tubing 24 where the remainder of the heat is transferred to the fresh fuel-air mixture flowing downwardly in line 32 to catalyst 34.

In substituting the heater shown in FIGURE 8 for the one in FIGURES 5 and 6, the gas flow is somewhat different in that the fuel-air mixture passes through tubing 32 the full length of catalyst bed 34, then flows upwardly through the catalyst, and heat is generated by oxidation of the fuel. At the top of catalyst bed 34, the resulting combustion products are conducted up the well and out of the system via the annulus between tubing 32 and tubing 24. It will be appreciated, of course, that the fluid flow can be reversed, i.e., the fuel-air mixture passed down the annulus between tubing strings 24 and 32 and back up through tubing 24. In the event thetemperature in the vicinity of tubing 24 becomes excessive, i.e., the fuel-air mixture is preheated to too high a temperature before contacting the catalyst bed, suitable insulation can be placed about tubing 24, thereby avoiding such undesirably high temperatures.

The apparatus shown in FIGURE 9 may be used with any type of heater of the general design illustrated in FIGURES 6 and 8. The modification shown in FIG- URE 9 comprising tubing 62, has metal seal 64, holding pipe 66 and maintains the latter substantially concentric with tubing 62 at or near the juncture of seal 64 with pipe 66 or perforations 68. This entire assembly may be attached at the lower end thereof to a heater such as shown in FIGURE 5. The modification in tubing arrangement, as shown in FIGURE 9 may be safely used where the combustible gas production from the oil is low enough that there will be no danger of formation of an explosive mixture in the casing. Thus, the fuel-air mixture flows downwardly to the heater via tubing 62 until it reaches seal 64 located, for example, 4 or 5 feet above the catalyst bed. The. entire flow is then directed into pipe 66 where it continues on its way and comes in contact with the oxidation catalyst, as previously described; Combustion or oxidation products are conducted away from the heater via annulus 70 and then leave the latter through perforations 68, traveling upwardly inside the casing and are then removed from the well.

The heat contained in the combustion products generated in the various ways mentioned above is transferred through the well fluids to formation 4, heating the oil therein and preventing parafiin or materials of a similar nature from solidifying at or near the formation face. The hot oil thus produced into the well and lifted to the surface via tubing 42, likewise, tends to prevent the deposition of paraffin in said tubingas well as in flow line 50.

The modification shown in FIGURE 10 eliminates the dual tubing arrangement used in the previously illustrated embodiment and is suitable for simultaneously pumping oil and heating an oil-containing formation penetrated by a well. In this. particular embodiment the assembly illustrated may replace the equipment shown in FIGURE 5. A heater 72 containing catalyst 34 is mounted on tubing 74* and located opposite perforations 8 and oilbearing formation 4. Inside tubing 74' is hollow sucker rod 76 carrying pump 46. A seal 78 is placed substantially midway of heater 72 to prevent flow of fluids upwardly through annulus 80. At the base of tubing 74 is standing valve 82 which allows hot produced oil to flow into the variable volume chamber defined by said valve and pump 46. Near the lower end of hollow sucker rod 76 are ports 84 which permit the fuel air mixture to fiow out of the rod and into lower ports 86 in heater 72. After the temperature of catalyst bed 34-has reached the desired level, air alone is sent down sucker rod 76 and the produced crude used as the fuel for heating. The

air rate is regulated to obtain substantially complete consumption of air in the catalyst bed to avoid burning or possible formation of explosive mixtures on the way to the surface. Produced oil flows into and through heater 7?. and out upper ports 88 along with oxidation products formed when the mixture of oil and air comes in contact with catalyst 34. The produced oil and combustion products are then removed from the well via annulus 90.

The fuel portion of the feed which is to be contacted with the catalyst in accordance with our invention may be selected from a wide variety of substances, such as, for example, light hydrocarbons, typically natural gas, propane, butane and unsaturated derivatives thereof, kerosene, crude oil, oxygenated organic chemicals, such as the lower molecular Weight alcohols, for example, methanol, and the like. Mixtures, of course, of two or more of the foregoing materials may be used-in gaseous or liquid formas the fuel component of the feed. In general, we prefer to employ air or oxygen-rich fuel mixtures, however, our invention also contemplates the use of fuel-rich mixtures. Tests using feed mixtures of propane and air and propylene and air were carried out under the conditions outlined below.

Table I 1 Platinum Oxide on Alumina. 2 Propane. 3 Propylene.

The above results, translated in terms of field requirements, show that to generate one million B.t.u./day, a total of 12 gallons of hydrocarbon and 87,000 s.c. f.d. of air are needed. To handle this feed mixture, approximately 0.14 cubic foot of catalyst is used. This corresponds to a column of catalyst 6 feet long in a 2-inch I.D. pipe.

The space velocities employed will vary with the nature of the fuel employed. Generally speaking, when methanol is used as the fuel, space velocities as high as 100,000 s.c.f.h. per cubic foot of catalyst may be employed. With fuels less readily oxidized, the space velocities ordinarily will be in the range of from about 10,000 to about 25,000 s.c.f.h. per cubic foot of catalyst. These figures, in both instances, refer to the combined fuel-air mixture.

The table below illustrates the temperature rise produced by contacting varying methane-air and propane-air mixtures with a supported platinum oxide catalyst so as to effect complete combustion of the fuel in an adiabatic system.

Table II Volume Ratio Temperature Volume Ratio Temperature s.c.f.-Air/CH Rise, F. s.c.f.-Air/ Rise, F.

Propane Preferred volume ratios of air to methane and air to propane (s.c.f.) are from about to 130 and from about 60 to about 200, respectively.

The effluent temperature from the catalyst bed can also be regulated by limiting the contact time of the fuel-air mixture with the catalyst so as to limit the amount of reaction obtained. Ordinarily, temperatures in excess of about 1500 F should not be employed.

. The catalysts used may be selected from a wide list of materials and form no part of our invention. Typically, catalysts suitable for oxidation of the feeds contemplated herein include the oxides of platinum, palladium, rhodium, etc. These oxides are preferably used in very dilute concentrations, e.g., 0.05 to about 0.5 weight percent, and may be supported on materials having a large surface area, such as pumice, aluminum oxide, metal wool, for example, stainless steel wool, and the like. Supported platinum oxide catalyst suitable for this purpose is manu factured by the Chemetron Corporation of Louisville, Ky., and is identified as catalyst (3-43. In operation, the portion of catalyst apparently entering into the oxidation reaction is that with which the feed mixture first comes in contact.

It is to be understood that while our invention is particularly applicable to the recovery of hydrocarbons from liquid petroleum reservoirs, it is equally suited to the recovery of valuable products from other sub-surface combustible materials such as, for example, oil shale, tar sand, coal and the like.

We claim:

1. A method for heating a subsurface formation containing combustible material, said formation being penetrated by a well, which comprises placing a body of an oxidation catalyst in said well at the approximate level of said formation, thereafter conducting a fuel-air mixture through said catalyst, said mixture being outside the explosive range, and passing the resulting hot oxidation products in heat exchange relation with said formation, said products having a temperature of from about 500 to about 1100 F.

2. The method of claim 1 in which the fuel component of said mixture is a light hydrocarbon.

3. The method of claim 1 in which the fuel component of said mixture is methanol.

4. The method of claim 1 in which the fuel component of said mixture is propane.

5. The method of claim 1 in which the fuel component of said mixture is propylene.

6. The method or" claim 1 in which the fuel component of said mixture is natural gas.

7. The method of claim 1 in which the combustible material is a heavy viscous crude.

8. The method of claim 7 in which said catalyst is in the form of a confined mass and the temperature of the oxidation products ranges from about 500 to about 1000 F.

9. In a process for recovering crude oil from a pumping well penetrating an oil-bearing formation and wherein production of said oil is hindered by the deposition of solid solid materials from said oil on the face of said formation, the improvement which comprises placing a body of oxidation catalyst in said Well and near the face of said formation, thereafter contacting a fuel-air mixture with said catalyst, said mixture being outside the explosive range, passing the resultant products of oxidation having a temperature of from about 500 to about 1100 F. in direct heat exchange relation with said formation whereby said deposition of materials is at least minimized, and recovering the heated oil via said Well from said formation.

10. The process of claim 9 in which the oil from said formation is employed as the fuel.

11. In a process for recovering crude oil from a pumping well penetrating an oil bearing formation and wherein production of said oil is hindered by the deposition of solid materials from said oil on the face of said formation, the improvement which comprises placing a confined mass of oxidation catalyst in said well and at the approximate level of said formation, thereafter contacting said catalyst with a fuel-oxygen-containing gas mixture having a composition sufficient to produce oxidation products having a temperature range from about 500 to about 1100 F., said mixture being outside of the explosive range, thereafter passing said products in heat exchange relationship with said formation,- and recovering the heated oil via said Well from said formation.

12. A method for treating an oil-bearing formation to promote the flow of oil therefrom, said formation being penetrated by a Well, which comprises placing a confined body of an oxidation catalyst in said Well and near the face of said formation, thereafter conducting a fuel-oxygen-containing gas mixture upwardly through said catalyst to produce oxidation products having a temperature of from about 500 to about 1100 F., said mixture being outside of the explosive'range, and bringing said products into indirect heat exchange with said mixture and with said formation.

13. In a method for heating to ignition temperature an underground formation containing a combustible material, said formation being penetrated by a Well, the improvement which comprises placing a confined body of an oxidation catalyst opposite said formation, thereafter conducting a fuel-oxygen-containing gas mixture through said catalyst in the absence of liquid in said well at the level of said body of catalyst, said mixture being outside the explosive range, and passing the resulting hot oxidation products in direct heat exchange with said formation until the latter has been heated to said ignition temperature.

References Cited by the Examiner UNITED STATES PATENTS 1,678,592 7/1928 Garner et al. 166-59 2,675,081 4/1954 NoWak 166-59 X 2,847,071 8/ 1958 De Priester 166-39 2,890,755 6/1959 Eurenius et a1 16659 2,997,105 8/1961 Campion et al 166-59 3,010,516 11/1961 Schleicher 16659 3,026,937 3/1962 Simm 166-39 3,055,427 9/1962 Pryor et al. 16659 3,070,178 12/1962. Graham et al 175-17 3,107,728 10/1963 Kehn 166-39 X 3,113,623 12/1963 Krueger 16659 3,127,935 4/1964 Poettman' et al 166-11 OTHER REFERENCES Haslazn and Russell: Fuels and Their Combustion, 1st edition, McGraw-Hill Book Co., New York, 1926 (pages 304 and 305) TP 318.113.

Hackhs Chemical Dictionary, 3rd edition (1944), The Blakiston Co., Phila, Pa., page 5 32.

The Condensed Chemical Dictionary, 6th edition, Reinhold Publishing Corporation, New York, 1961, pages 51, 52 and 794.

CHARLES E. OCONNELL, Primary Examiner.

BENJAMIN HERSH, Examiner.

Claims (1)

1. A METHOD FOR HEATING A SUBSURFACE FORMATION CONTAINING COMBUSTIBLE MATERIAL, SAID FORMATION BEING PENETRATED BY A WELL, WHICH COMPRISES PLACING A BODY OF AN OXIDATION CATALYST IN SAID WELL AT THE APPROXIMATE LEVEL OF SAID FORMATION, THEREAFTER CONDUCTING A FUEL-AIR MIXTURE THROUGH SAID CATALYST, SAID MIXTURE BEING OUTSIDE THE EXPLOSIVE RANGE, AND PASSING THE RESULTING HOT OXIDATION PRODUCTS IN HEAT EXCHANGE RELATION WITH SAID FORMATION SAID PRODUCTS HAVING A TEMPERATURE OF FROM ABOUT 500* TO ABOUT 1100*F.
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Cited By (35)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3376932A (en) * 1966-03-04 1968-04-09 Pan American Petroleum Corp Catalytic heater
US3420300A (en) * 1966-10-27 1969-01-07 Sinclair Research Inc Method and apparatus for heating a subsurface formation
US3481399A (en) * 1968-06-10 1969-12-02 Pan American Petroleum Corp Recovery of oil by flashing of heated connate water
US3497000A (en) * 1968-08-19 1970-02-24 Pan American Petroleum Corp Bottom hole catalytic heater
US3680636A (en) * 1969-12-30 1972-08-01 Sun Oil Co Method and apparatus for ignition and heating of earth formations
US3804163A (en) * 1972-06-08 1974-04-16 Sun Oil Co Catalytic wellbore heater
US3817332A (en) * 1969-12-30 1974-06-18 Sun Oil Co Method and apparatus for catalytically heating wellbores
US3880235A (en) * 1969-12-30 1975-04-29 Sun Oil Co Delaware Method and apparatus for igniting well heaters
US4250962A (en) * 1979-12-14 1981-02-17 Gulf Research & Development Company In situ combustion process for the recovery of liquid carbonaceous fuels from subterranean formations
FR2573049A1 (en) * 1984-11-14 1986-05-16 Fournier Lab Sa packaging box
US4687491A (en) * 1981-08-21 1987-08-18 Dresser Industries, Inc. Fuel admixture for a catalytic combustor
US4930454A (en) * 1981-08-14 1990-06-05 Dresser Industries, Inc. Steam generating system
US5082055A (en) * 1990-01-24 1992-01-21 Indugas, Inc. Gas fired radiant tube heater
US5224542A (en) * 1990-01-24 1993-07-06 Indugas, Inc. Gas fired radiant tube heater
US20020029881A1 (en) * 2000-04-24 2002-03-14 De Rouffignac Eric Pierre In situ thermal processing of a hydrocarbon containing formation using conductor in conduit heat sources
US20020029885A1 (en) * 2000-04-24 2002-03-14 De Rouffignac Eric Pierre In situ thermal processing of a coal formation using a movable heating element
US20030062154A1 (en) * 2000-04-24 2003-04-03 Vinegar Harold J. In situ production of synthesis gas from a hydrocarbon containing formation through a heat source wellbore
US20030062164A1 (en) * 2000-04-24 2003-04-03 Wellington Scott Lee In situ thermal processing of a hydrocarbon containing formation to produce nitrogen containing formation fluids
US20030066644A1 (en) * 2000-04-24 2003-04-10 Karanikas John Michael In situ thermal processing of a coal formation using a relatively slow heating rate
US20030085034A1 (en) * 2000-04-24 2003-05-08 Wellington Scott Lee In situ thermal processing of a coal formation to produce pyrolsis products
US20030100451A1 (en) * 2001-04-24 2003-05-29 Messier Margaret Ann In situ thermal recovery from a relatively permeable formation with backproduction through a heater wellbore
US20030130136A1 (en) * 2001-04-24 2003-07-10 Rouffignac Eric Pierre De In situ thermal processing of a relatively impermeable formation using an open wellbore
US20030141066A1 (en) * 2001-04-24 2003-07-31 Karanikas John Michael In situ thermal processing of an oil shale formation while inhibiting coking
US20030183390A1 (en) * 2001-10-24 2003-10-02 Peter Veenstra Methods and systems for heating a hydrocarbon containing formation in situ with an opening contacting the earth's surface at two locations
US20060260814A1 (en) * 2005-05-23 2006-11-23 Pfefferle William C Reducing the energy requirements for the production of heavy oil
US20080296018A1 (en) * 2007-05-29 2008-12-04 Zubrin Robert M System and method for extracting petroleum and generating electricity using natural gas or local petroleum
US20090229815A1 (en) * 2006-03-29 2009-09-17 Pioneer Energy, Inc. Apparatus and Method for Extracting Petroleum from Underground Sites Using Reformed Gases
US20090236093A1 (en) * 2006-03-29 2009-09-24 Pioneer Energy, Inc. Apparatus and Method for Extracting Petroleum from Underground Sites Using Reformed Gases
US20090321073A1 (en) * 2006-01-03 2009-12-31 Pfefferle William C Method for in-situ combustion of in-place oils
US20100108305A1 (en) * 2005-05-23 2010-05-06 Pfefferle William C Reducing the energy requirements for the production of heavy oil
US7942203B2 (en) 2003-04-24 2011-05-17 Shell Oil Company Thermal processes for subsurface formations
US8224163B2 (en) 2002-10-24 2012-07-17 Shell Oil Company Variable frequency temperature limited heaters
US8616294B2 (en) 2007-05-20 2013-12-31 Pioneer Energy, Inc. Systems and methods for generating in-situ carbon dioxide driver gas for use in enhanced oil recovery
US8785699B2 (en) 2008-07-17 2014-07-22 Pioneer Energy, Inc. Methods of higher alcohol synthesis
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 (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US1678592A (en) * 1923-02-03 1928-07-24 Standard Oil Dev Co Art of treating oil wells
US2675081A (en) * 1950-10-23 1954-04-13 Union Oil Co Method and apparatus for pumping and heating oil wells
US2847071A (en) * 1955-09-20 1958-08-12 California Research Corp Methods of igniting a gas air-burner utilizing pelletized phosphorus
US2890755A (en) * 1953-12-19 1959-06-16 Svenska Skifferolje Ab Apparatus for recovering combustible substances from subterraneous deposits in situ
US2997105A (en) * 1956-10-08 1961-08-22 Pan American Petroleum Corp Burner apparatus
US3010516A (en) * 1957-11-18 1961-11-28 Phillips Petroleum Co Burner and process for in situ combustion
US3026937A (en) * 1957-05-17 1962-03-27 California Research Corp Method of controlling an underground combustion zone
US3055427A (en) * 1959-07-13 1962-09-25 Phillips Petroleum Co Self contained igniter-burner and process
US3070178A (en) * 1961-08-28 1962-12-25 Jersey Prod Res Co Method of drilling wells with air
US3107728A (en) * 1961-10-16 1963-10-22 Jersey Prod Res Co Down-hole heater
US3113623A (en) * 1959-07-20 1963-12-10 Union Oil Co Apparatus for underground retorting
US3127935A (en) * 1960-04-08 1964-04-07 Marathon Oil Co In situ combustion for oil recovery in tar sands, oil shales and conventional petroleum reservoirs

Patent Citations (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US1678592A (en) * 1923-02-03 1928-07-24 Standard Oil Dev Co Art of treating oil wells
US2675081A (en) * 1950-10-23 1954-04-13 Union Oil Co Method and apparatus for pumping and heating oil wells
US2890755A (en) * 1953-12-19 1959-06-16 Svenska Skifferolje Ab Apparatus for recovering combustible substances from subterraneous deposits in situ
US2847071A (en) * 1955-09-20 1958-08-12 California Research Corp Methods of igniting a gas air-burner utilizing pelletized phosphorus
US2997105A (en) * 1956-10-08 1961-08-22 Pan American Petroleum Corp Burner apparatus
US3026937A (en) * 1957-05-17 1962-03-27 California Research Corp Method of controlling an underground combustion zone
US3010516A (en) * 1957-11-18 1961-11-28 Phillips Petroleum Co Burner and process for in situ combustion
US3055427A (en) * 1959-07-13 1962-09-25 Phillips Petroleum Co Self contained igniter-burner and process
US3113623A (en) * 1959-07-20 1963-12-10 Union Oil Co Apparatus for underground retorting
US3127935A (en) * 1960-04-08 1964-04-07 Marathon Oil Co In situ combustion for oil recovery in tar sands, oil shales and conventional petroleum reservoirs
US3070178A (en) * 1961-08-28 1962-12-25 Jersey Prod Res Co Method of drilling wells with air
US3107728A (en) * 1961-10-16 1963-10-22 Jersey Prod Res Co Down-hole heater

Cited By (143)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3376932A (en) * 1966-03-04 1968-04-09 Pan American Petroleum Corp Catalytic heater
US3420300A (en) * 1966-10-27 1969-01-07 Sinclair Research Inc Method and apparatus for heating a subsurface formation
US3481399A (en) * 1968-06-10 1969-12-02 Pan American Petroleum Corp Recovery of oil by flashing of heated connate water
US3497000A (en) * 1968-08-19 1970-02-24 Pan American Petroleum Corp Bottom hole catalytic heater
US3817332A (en) * 1969-12-30 1974-06-18 Sun Oil Co Method and apparatus for catalytically heating wellbores
US3680636A (en) * 1969-12-30 1972-08-01 Sun Oil Co Method and apparatus for ignition and heating of earth formations
US3880235A (en) * 1969-12-30 1975-04-29 Sun Oil Co Delaware Method and apparatus for igniting well heaters
US3804163A (en) * 1972-06-08 1974-04-16 Sun Oil Co Catalytic wellbore heater
US4250962A (en) * 1979-12-14 1981-02-17 Gulf Research & Development Company In situ combustion process for the recovery of liquid carbonaceous fuels from subterranean formations
US4930454A (en) * 1981-08-14 1990-06-05 Dresser Industries, Inc. Steam generating system
US4687491A (en) * 1981-08-21 1987-08-18 Dresser Industries, Inc. Fuel admixture for a catalytic combustor
FR2573049A1 (en) * 1984-11-14 1986-05-16 Fournier Lab Sa packaging box
US5082055A (en) * 1990-01-24 1992-01-21 Indugas, Inc. Gas fired radiant tube heater
US5224542A (en) * 1990-01-24 1993-07-06 Indugas, Inc. Gas fired radiant tube heater
US20020029882A1 (en) * 2000-04-24 2002-03-14 Rouffignac Eric Pierre De In situ thermal processing of a hydrocarbon containing formation leaving one or more selected unprocessed areas
US20020029884A1 (en) * 2000-04-24 2002-03-14 De Rouffignac Eric Pierre In situ thermal processing of a coal formation leaving one or more selected unprocessed areas
US20020029885A1 (en) * 2000-04-24 2002-03-14 De Rouffignac Eric Pierre In situ thermal processing of a coal formation using a movable heating element
US20020029881A1 (en) * 2000-04-24 2002-03-14 De Rouffignac Eric Pierre In situ thermal processing of a hydrocarbon containing formation using conductor in conduit heat sources
US20020033256A1 (en) * 2000-04-24 2002-03-21 Wellington Scott Lee In situ thermal processing of a hydrocarbon containing formation with a selected hydrogen to carbon ratio
US20020035307A1 (en) * 2000-04-24 2002-03-21 Vinegar Harold J. In situ thermal processing of a coal formation, in situ production of synthesis gas, and carbon dioxide sequestration
US20020033253A1 (en) * 2000-04-24 2002-03-21 Rouffignac Eric Pierre De In situ thermal processing of a hydrocarbon containing formation using insulated conductor heat sources
US20020034380A1 (en) * 2000-04-24 2002-03-21 Maher Kevin Albert In situ thermal processing of a coal formation with a selected moisture content
US20020033257A1 (en) * 2000-04-24 2002-03-21 Shahin Gordon Thomas In situ thermal processing of hydrocarbons within a relatively impermeable formation
US20020033255A1 (en) * 2000-04-24 2002-03-21 Fowler Thomas David In situ thermal processing of a hydrocarbon containing formation in a hydrogen-rich environment
US20020036084A1 (en) * 2000-04-24 2002-03-28 Vinegar Harold J. In situ thermal processing of a hydrocarbon containing formation to form a substantially uniform, high permeability formation
US20020036089A1 (en) * 2000-04-24 2002-03-28 Vinegar Harold J. In situ thermal processing of a hydrocarbon containing formation using distributed combustor heat sources
US20020038069A1 (en) * 2000-04-24 2002-03-28 Wellington Scott Lee In situ thermal processing of a coal formation to produce a mixture of olefins, oxygenated hydrocarbons, and aromatic hydrocarbons
US20020036103A1 (en) * 2000-04-24 2002-03-28 Rouffignac Eric Pierre De In situ thermal processing of a coal formation by controlling a pressure of the formation
US20020036083A1 (en) * 2000-04-24 2002-03-28 De Rouffignac Eric Pierre In situ thermal processing of a hydrocarbon containing formation with heat sources located at an edge of a formation layer
US20020039486A1 (en) * 2000-04-24 2002-04-04 Rouffignac Eric Pierre De In situ thermal processing of a coal formation using heat sources positioned within open wellbores
US20020038712A1 (en) * 2000-04-24 2002-04-04 Vinegar Harold J. In situ production of synthesis gas from a coal formation through a heat source wellbore
US20020038711A1 (en) * 2000-04-24 2002-04-04 Rouffignac Eric Pierre De In situ thermal processing of a hydrocarbon containing formation using heat sources positioned within open wellbores
US20020038705A1 (en) * 2000-04-24 2002-04-04 Wellington Scott Lee In situ thermal processing of a hydrocarbon containing formation to produce a mixture with a selected hydrogen content
US20020038709A1 (en) * 2000-04-24 2002-04-04 Wellington Scott Lee In situ thermal processing of a hydrocarbon containing formation using a natural distributed combustor
US20020040177A1 (en) * 2000-04-24 2002-04-04 Maher Kevin Albert In situ thermal processing of a hydrocarbon containig formation, in situ production of synthesis gas, and carbon dioxide sequestration
US20020038710A1 (en) * 2000-04-24 2002-04-04 Maher Kevin Albert In situ thermal processing of a hydrocarbon containing formation having a selected total organic carbon content
US20020040779A1 (en) * 2000-04-24 2002-04-11 Wellington Scott Lee In situ thermal processing of a hydrocarbon containing formation to produce a mixture containing olefins, oxygenated hydrocarbons, and/or aromatic hydrocarbons
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US20020043367A1 (en) * 2000-04-24 2002-04-18 Rouffignac Eric Pierre De In situ thermal processing of a hydrocarbon containing formation to increase a permeability of the formation
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US20020046832A1 (en) * 2000-04-24 2002-04-25 Etuan Zhang In situ thermal processing of a hydrocarbon containing formation to convert a selected amount of total organic carbon into hydrocarbon products
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US20020052297A1 (en) * 2000-04-24 2002-05-02 Rouffignac Eric Pierre De In situ thermal processing of a hydrocarbon containing formation by controlling a pressure of the formation
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US20020050356A1 (en) * 2000-04-24 2002-05-02 Vinegar Harold J. In situ thermal processing of a coal formation with a selected oxygen content and/or selected O/C ratio
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US20020053435A1 (en) * 2000-04-24 2002-05-09 Vinegar Harold J. In situ thermal processing of a hydrocarbon containing formation using a relatively slow heating rate
US20020053429A1 (en) * 2000-04-24 2002-05-09 Stegemeier George Leo In situ thermal processing of a hydrocarbon containing formation using pressure and/or temperature control
US20020053432A1 (en) * 2000-04-24 2002-05-09 Berchenko Ilya Emil In situ thermal processing of a hydrocarbon containing formation using repeating triangular patterns of heat sources
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US20020062051A1 (en) * 2000-04-24 2002-05-23 Wellington Scott L. In situ thermal processing of a hydrocarbon containing formation with a selected moisture content
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US20020191969A1 (en) * 2000-04-24 2002-12-19 Wellington Scott Lee In situ thermal processing of a coal formation in reducing environment
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US20030019626A1 (en) * 2000-04-24 2003-01-30 Vinegar Harold J. In situ thermal processing of a coal formation with a selected hydrogen content and/or selected H/C ratio
US20030024699A1 (en) * 2000-04-24 2003-02-06 Vinegar Harold J. In situ production of synthesis gas from a coal formation, the synthesis gas having a selected H2 to CO ratio
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
US20030062154A1 (en) * 2000-04-24 2003-04-03 Vinegar Harold J. In situ production of synthesis gas from a hydrocarbon containing formation through a heat source wellbore
US20030062164A1 (en) * 2000-04-24 2003-04-03 Wellington Scott Lee In situ thermal processing of a hydrocarbon containing formation to produce nitrogen containing formation fluids
US20030066644A1 (en) * 2000-04-24 2003-04-10 Karanikas John Michael In situ thermal processing of a coal formation using a relatively slow heating rate
US20030085034A1 (en) * 2000-04-24 2003-05-08 Wellington Scott Lee In situ thermal processing of a coal formation to produce pyrolsis products
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
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
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
US20030141065A1 (en) * 2000-04-24 2003-07-31 Karanikas John Michael In situ thermal processing of hydrocarbons within a relatively permeable formation
US20030164238A1 (en) * 2000-04-24 2003-09-04 Vinegar Harold J. In situ thermal processing of a coal formation using a controlled heating rate
US20030164234A1 (en) * 2000-04-24 2003-09-04 De Rouffignac Eric Pierre In situ thermal processing of a hydrocarbon containing formation using a movable heating element
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
US20030213594A1 (en) * 2000-04-24 2003-11-20 Shell Oil Company In situ thermal processing of a hydrocarbon containing formation to produce a mixture with a selected hydrogen content
US20040015023A1 (en) * 2000-04-24 2004-01-22 Wellington Scott Lee In situ thermal processing of a hydrocarbon containing formation to produce a hydrocarbon condensate
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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
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US20040069486A1 (en) * 2000-04-24 2004-04-15 Vinegar Harold J. In situ thermal processing of a coal formation and tuning production
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
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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
US20040108111A1 (en) * 2000-04-24 2004-06-10 Vinegar Harold J. In situ thermal processing of a coal formation to increase a permeability/porosity 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
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
US6763886B2 (en) 2000-04-24 2004-07-20 Shell Oil Company In situ thermal processing of a coal formation with carbon dioxide sequestration
US20030051872A1 (en) * 2000-04-24 2003-03-20 De Rouffignac Eric Pierre In situ thermal processing of a coal formation with heat sources located at an edge of a coal layer
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
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
US20030100451A1 (en) * 2001-04-24 2003-05-29 Messier Margaret Ann In situ thermal recovery from a relatively permeable formation with backproduction through a heater wellbore
US20030141066A1 (en) * 2001-04-24 2003-07-31 Karanikas John Michael In situ thermal processing of an oil shale formation while inhibiting coking
US6877555B2 (en) * 2001-04-24 2005-04-12 Shell Oil Company In situ thermal processing of an oil shale formation while inhibiting coking
US20030130136A1 (en) * 2001-04-24 2003-07-10 Rouffignac Eric Pierre De In situ thermal processing of a relatively impermeable formation using an open wellbore
US6782947B2 (en) 2001-04-24 2004-08-31 Shell Oil Company In situ thermal processing of a relatively impermeable formation to increase permeability of the formation
US20030183390A1 (en) * 2001-10-24 2003-10-02 Peter Veenstra Methods and systems for heating a hydrocarbon containing formation in situ with an opening contacting the earth's surface at two locations
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
US8238730B2 (en) 2002-10-24 2012-08-07 Shell Oil Company High voltage 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
US20060260814A1 (en) * 2005-05-23 2006-11-23 Pfefferle William C Reducing the energy requirements for the production of heavy oil
US7665525B2 (en) * 2005-05-23 2010-02-23 Precision Combustion, Inc. Reducing the energy requirements for the production of heavy oil
US20100108305A1 (en) * 2005-05-23 2010-05-06 Pfefferle William C Reducing the energy requirements for the production of heavy oil
US7874350B2 (en) 2005-05-23 2011-01-25 Precision Combustion, Inc. Reducing the energy requirements for the production of heavy oil
US20090321073A1 (en) * 2006-01-03 2009-12-31 Pfefferle William C Method for in-situ combustion of in-place oils
US8167036B2 (en) 2006-01-03 2012-05-01 Precision Combustion, Inc. Method for in-situ combustion of in-place oils
US20090229815A1 (en) * 2006-03-29 2009-09-17 Pioneer Energy, Inc. Apparatus and Method for Extracting Petroleum from Underground Sites Using Reformed Gases
US20090236093A1 (en) * 2006-03-29 2009-09-24 Pioneer Energy, Inc. Apparatus and Method for Extracting Petroleum from Underground Sites Using Reformed Gases
US8602095B2 (en) * 2006-03-29 2013-12-10 Pioneer Energy, Inc. Apparatus and method for extracting petroleum from underground sites using reformed gases
US9605522B2 (en) 2006-03-29 2017-03-28 Pioneer Energy, Inc. Apparatus and method for extracting petroleum from underground sites using reformed gases
US9605523B2 (en) 2007-05-20 2017-03-28 Pioneer Energy, Inc. Systems and methods for generating in-situ carbon dioxide driver gas for use in enhanced oil recovery
US8616294B2 (en) 2007-05-20 2013-12-31 Pioneer Energy, Inc. Systems and methods for generating in-situ carbon dioxide driver gas for use in enhanced oil recovery
US20080296018A1 (en) * 2007-05-29 2008-12-04 Zubrin Robert M System and method for extracting petroleum and generating electricity using natural gas or local petroleum
US8785699B2 (en) 2008-07-17 2014-07-22 Pioneer Energy, Inc. Methods of higher alcohol synthesis
US10047594B2 (en) 2012-01-23 2018-08-14 Genie Ip B.V. Heater pattern for in situ thermal processing of a subsurface hydrocarbon containing formation

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