CA2579496A1 - Subsurface electrical heaters using nitride insulation - Google Patents

Subsurface electrical heaters using nitride insulation Download PDF

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Publication number
CA2579496A1
CA2579496A1 CA002579496A CA2579496A CA2579496A1 CA 2579496 A1 CA2579496 A1 CA 2579496A1 CA 002579496 A CA002579496 A CA 002579496A CA 2579496 A CA2579496 A CA 2579496A CA 2579496 A1 CA2579496 A1 CA 2579496A1
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Prior art keywords
formation
conductor
electrical
temperature
heat
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CA002579496A
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French (fr)
Inventor
Harold J. Vinegar
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Shell Internationale Research Maatschappij BV
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Classifications

    • 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
    • E21B36/04Heating, cooling, insulating arrangements for boreholes or wells, e.g. for use in permafrost zones using electrical heaters
    • 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
    • E21B43/00Methods or apparatus for obtaining oil, gas, water, soluble or meltable materials or a slurry of minerals from wells
    • E21B43/12Methods or apparatus for controlling the flow of the obtained fluid to or in wells
    • 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
    • E21B43/00Methods or apparatus for obtaining oil, gas, water, soluble or meltable materials or a slurry of minerals from wells
    • E21B43/12Methods or apparatus for controlling the flow of the obtained fluid to or in wells
    • E21B43/121Lifting well fluids
    • E21B43/122Gas lift
    • 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
    • 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
    • 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
    • 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 DRILLING; MINING
    • E21BEARTH DRILLING, e.g. DEEP 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
    • E21B43/2405Enhanced recovery methods for obtaining hydrocarbons using heat, e.g. steam injection in association with fracturing or crevice forming processes
    • 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
    • E21B43/00Methods or apparatus for obtaining oil, gas, water, soluble or meltable materials or a slurry of minerals from wells
    • E21B43/34Arrangements for separating materials produced by the well
    • E21B43/38Arrangements for separating materials produced by the well in the well
    • HELECTRICITY
    • H05ELECTRIC TECHNIQUES NOT OTHERWISE PROVIDED FOR
    • H05BELECTRIC HEATING; ELECTRIC LIGHT SOURCES NOT OTHERWISE PROVIDED FOR; CIRCUIT ARRANGEMENTS FOR ELECTRIC LIGHT SOURCES, IN GENERAL
    • H05B3/00Ohmic-resistance heating
    • H05B3/10Heater elements characterised by the composition or nature of the materials or by the arrangement of the conductor
    • H05B3/12Heater elements characterised by the composition or nature of the materials or by the arrangement of the conductor characterised by the composition or nature of the conductive material
    • H05B3/14Heater elements characterised by the composition or nature of the materials or by the arrangement of the conductor characterised by the composition or nature of the conductive material the material being non-metallic
    • H05B3/141Conductive ceramics, e.g. metal oxides, metal carbides, barium titanate, ferrites, zirconia, vitrous compounds

Abstract

The invention provides a system that includes an electrical conductor configured to generate an electrically resistive heat output during application of electrical current to the electrical conductor. An electrical insulator at least partially surrounds the electrical conductor. The electrical insulator includes a nitride. A sheath at least partially surrounds the electrical insulator.

Description

SUBSURFACE ELECTRICAL HEATERS USING NITRIDE INSULATION
BACKGROUND
Field of the Invention The present invention relates generally to methods and systems for production of hydrocarbons, hydrogen, and/or other products from various subsurface formations such as hydrocarbon containing formations.
In particular, certain embodiments described herein relate to heaters with nitride electrical insulation.
Description of Related Art Hydrocarbons obtained from subterranean formations are often used as energy resources, as feedstocks, and as consumer products. Conceins over depletion of available hydrocarbon resources and changes in the overall quality of produced hydrocarbons have led to development of processes for more efficient recovery, processing, and/or use of available hydrocarbon resources. In situ processes may be used to remove hydrocarbon materials from subterranean formations. Chemical and/or physical properties of hydrocarbon material within subterranean formations may need to be changed to allow hydrocarbon material to be more easily removed from the subterranean formations. Chemical and physical changes may include: in situ reactions that produce removable fluids, composition changes, solubility changes, density changes, phase changes, and/or viscosity changes of the hydrocarbon material within the foimation. A fluid may be, but is not limited to, a gas, a liquid, an emulsion, a slurry, and/or a stream of solid particles that has flow characteristics similar to liquid flow.
Electric heaters may be used to heat the subterranean formation by radiation and/or conduction. U.S.
Patent No. 2,548,360 to Germain describes an electric heater adapted to be lowered into the casing of a well and submerged in the oil in such a manner and to such effect that heavy gravity oil which is ordinarily incapable of being pumped from the well in its natural state, at least in sufficient volume to render a well profitable or efficient, may be heated and thereby thinned to a consistency capable of being pumped in fu11 and profitable volume. U.S. Patent No. 4,716,960 to Eastlund et al. describes electrically heat the tubing of a petroleum well by passing current through the tubing to prevent formation of solids such as paraffins. U.S. Patent No.
5,065,818 to Van Egmond describes a subterranean heater which does not require a casing.
U.S. Patent No. 6,023,554 to Vinegar et al. describes a heating element, a casing surrounding the heating element, and support material separating the resistance heating element and the casing. The support material is translucent to radiant energy generated by the resistance heating element so that heat transfer from the electrical heating element to the casing is both radiant and conductive.
The heater element is useful as a well heater for such purposes as thermal recovery of hydrocarbons and soil remediation.
U.S. Patent No. 4,570,715 to Van Meurs et al. describes an electric heating element. An electrical heater is arranged to have at least one heating element within the interval to be heated. Said heating element or elements consist essentially of (a) an electrically conductive core or conductor which has a relatively low resistance at a high temperature, (b) a core-surrounding insulating material having properties of electrical resistance, compressive strength and heat conductivity which are relatively high at a high temperature, and (c) a core and insulation-surrounding metal sheath having properties of tensile strength, creep resistance, and softening resistance which are relatively high at a high temperature. Said electrical heater is also arranged so that, along the interval to be heated, the heater has a pattern of electrical resistance with distance, (for example, due to combinations of core cross-sectional area and resistance per unit length) which is correlated with the pattern of heat conductivity with distance along the interval of earth formation to be heated.
Certain heaters use insulators that are not very dense and have low tensile strength, low flexural mechanical strength, and/or low thermal impact stress characteristics. Also, certain heaters may be used at temperatures high enough to cause breakdown or failure of certain types of insulators. Thus, insulators for use in certain heaters described herein are very dense materials with high tensile strength, high flexural mechanical strength, and high thermal impact stress characteristics. Certain insulators described herein are also excellent high temperature electrical insulators.
Summary of the Invention The invention provides a system, comprising: an electrical conductor configured to generate an electrically resistive heat output during application of electrical current to the electrical conductor;an electrical insulator at least partially surrounding the electrical conductor, wherein the electrical insulator comprises a nitride; and a sheath at least partially surrounding the electrical insulator.
The invention also provides in combination with the above invention wherein (a) the nitride is silicon nitride or boron nitride; (b) the electrical conductor is a copper-nickel alloy; and/or (c) the sheath is a corrosion-resistant material.
The invention also provides an in situ method for heating a formation using the system of the above invention.
Brief Description of the Drawings Advantages of the present invention will become apparent to those skilled in the art with the benefit of the following detailed description and upon reference to the accompanying drawings in which:
FIG. 1 depicts an illustration of stages of heating hydrocarbons in the formation.
FIG. 2 shows a schematic view of an embodiment of a portion of an in situ conversion system for treating a hydrocarbon containing formation.
FIGS. 3, 4, and 5 depict cross-sectional representations of an embodiment of a temperature limited heater with an outer conductor having a ferromagnetic section and a non-ferromagnetic section.
FIGS. 6, 7, 8, and 9 depict cross-sectional representations of an embodiment of a temperature limited heater with an outer conductor having a ferromagnetic section and a non-feiromagnetic section placed inside a sheath.
FIGS. 10, 11, and 12 depict cross-sectional representations of an embodiment of a temperature limited heater with an outer conductor.
FIGS. 13, 14, 15, and 16 depict cross-sectional representations of an embodiment of a temperature limited heater.
FIGS. 17A and 17B depict cross-sectional representations of an einbodiment of a temperature limited heater.
FIGS. 18A and 18B depict cross-sectional representations of an embodiment of a temperature limited heater.
FIG. 19 depicts a cross-sectional representation of an embodiment of a conductor-in-conduit heat source.
FIG. 20 depicts a cross-sectional representation of an embodiment of a removable conductor-in-conduit heat source.
FIG. 21A and FIG. 21B depict an embodiment of an insulated conductor heater.
FIG. 22 depicts an embodiment of a conductor-in-conduit temperature limited heater.
FIG. 23 depicts an enibodiment of a three-phase temperature limited heater, with a portion shown in cross section.
FIG. 24 depicts an embodiment of a three-phase temperature limited heater, with a portion shown in cross section.
FIG. 25 depicts leakage current measurements versus voltage for alumina and silicon nitride centralizers at selected temperatures.
FIG. 26 depicts leakage current measurements versus temperature for two different types of silicon nitride.
While the invention is susceptible to various modifications and alternative forms, specific embodiments thereof are shown by way of example in the drawings and may herein be described in detail. The drawings may not be to scale. It should be understood, however, that the drawings and detailed description thereto are not intended to limit the invention to the particular form disclosed, but on the contrary, the intention is to cover all modifications, equivalents and alternatives falling within the spirit and scope of the present invention as defined by the appended claims.
Detailed Description of the Invention The above problems may be addressed using systems, methods, and heaters described herein. For example, a system includes an electrical conductor configured to generate an electrically resistive heat output during application of electrical current to the electrical conductor. An electrical insulator at least partially surrounds and is in direct physical contact with the electrical conductor. The electrical insulator may include a nitride. A sheath at least partially surrounds and is in direct physical contact with the electrical insulator.
The following description generally relates to systems and methods for treating hydrocarbons in the formations. Such formations may be treated to yield hydrocarbon products, hydrogen, and other products.
Terms used herein are defined as follows.
"Hydrocarbons" are generally defined as molecules formed primarily by carbon and hydrogen atoms.
Hydrocarbons may also include other elements such as, but not limited to, halogens, metallic elements, nitrogen, oxygen, and/or sulfur. Hydrocarbons may be, but are not limited to, kerogen, bitumen, pyrobitumen, oils, natural mineral waxes, and asphaltites. Hydrocarbons may be located in or adjacent to mineral matrices in the earth. Matrices may include, but are not limited to, sedimentary rock, sands, silicilytes, carbonates, diatomites, and other porous media. "Hydrocarbon fluids" are fluids that include hydrocarbons. Hydrocarbon fluids may include, entrain, or be entrained in non-hydrocarbon fluids (for example, hydrogen, nitrogen, carbon monoxide, carbon dioxide, hydrogen sulfide, water, and ammonia).
"API gravity" refers to API gravity at 15.5 C (60 F). API gravity is as determined by ASTM
Method D6822. "ASTM" refers to American Standard Testing and Materials.
A "formation" includes one or more hydrocarbon containing layers, one or more non-hydrocarbon layers, an overburden, and/or an underburden. The "overburden" and/or the "underburden" include one or more different types of impermeable materials. For example, overburden and/or underburden may include rock, shale, mudstone, or wet/tight carbonate. In some embodiments of in situ conversion processes, the overburden and/or the underburden may include a hydrocarbon containing layer or hydrocarbon containing layers that are relatively impermeable and are not subjected to temperatures during in situ conversion processing that results in significant characteristic changes of the hydrocarbon containing layers of the overburden and/or the underburden. For example, the underburden may contain shale or mudstone, but the underburden is not allowed to heat to pyrolysis temperatures during the in situ conversion process. In some cases, the overburden and/or the underburden may be soinewhat permeable.
"Formation fluids" and "produced fluids" refer to fluids removed from the formation and may include pyrolyzation fluid, synthesis gas, mobilized hydrocarbon, and water (steam).
Formation fluids may include hydrocarbon fluids as well as non-hydrocarbon fluids.
A "heater" is any system for generating heat in a well or a near wellbore region. Heaters inay be, but are not limited to, electric heaters, circulated heat transfer fluid or steam, burners, combustors that react with material in or produced fiom the formation, and/or combinations thereof. The term "wellbore" refers to a hole in the formation inade by drilling or insertion of a conduit into the formation. As used herein, the terms "well"
and "opening", when referring to an opening in the formation, may be used interchangeably with the term "wellbore".
"Temperature limited heater" generally refers to a heater that regulates heat output (for example, reduces heat output) above a specified temperature without the use of external controls such as temperature controllers, power regulators, rectifiers, or other devices. Temperature limited heaters may be AC (alternating current) or inodulated (for example, "chopped") DC (direct current) powered electrical resistance heaters.
"Curie temperature" is the temperature above which a ferromagnetic material loses all of its ferromagnetic properties. In addition to losing all of its ferromagnetic properties above the Curie temperature, the ferromagnetic material begins to lose its ferromagnetic properties when an increasing electrical current is passed through the ferromagnetic ma.terial.
"Time-varying current" refers to an electrical current that has a magnitude that varys with time. Time-varying current includes both alternating current (AC) and modulated direct current (DC).
"Alternating current (AC)" refers to a time-varying current that reverses direction substantially sinusoidally. AC produces skin effect electricity flow in a ferromagnetic conductor.
"Modulated direct current (DC)" refers to any substantially non-sinusoidal time-varying current that produces skin effect electricity flow in a ferromagnetic conductor.
"Tumdown ratio" for the temperature limited heater is the ratio of the highest AC or modulated DC
resistance below the Curie temperature to the lowest resistance above the Curie temperature for a given current.
"Nitride" refers to a compound of nitrogen and one or more other elements of the Periodic Table.
Nitrides include, but are not limited to, silica nitride, boron nitride, or alumina nitride.
"Pyrolysis" is the breaking of chemical bonds due to the application of heat.
Pyrolysis includes transforming a compound into one or more other substances by heat alone. Heat may be transferred to a section of the formation to cause pyrolysis. "Pyrolyzation fluids" or "pyrolysis products" refers to fluid produced during pyrolysis of hydrocarbons. Fluid produced by pyrolysis reactions may mix with other fluids in the formation. The mixture would be considered pyrolyzation fluid or pyrolyzation product. Pyrolyzation fluids include, but are not limited to, hydrocarbons, hydrogen, carbon dioxide, carbon monoxide, hydrogen sulfide, ammonia, nitrogen, water, and mixtures thereof.
"Condensable hydrocarbons" are hydrocarbons that condense at 25 C and 101 kPa absolute pressure.
Condensable hydrocarbons may include a mixture of hydrocarbons having carbon numbers greater than 4.
"Non-condensable hydrocarbons" are hydrocarbons that do not condense at 25 C
and 101 kPa absolute pressure. Non-condensable hydrocarbons may include hydrocarbons having carbon numbers less than 5.
Hydrocarbons in formations may be treated in various ways to produce many different products. In certain embodiments, such formations are treated in stages. FIG. 1 illustrates several stages of heating a portion of the formation that contains hydrocarbons. FIG. 1 also depicts an example of yield ("Y") in barrels of oil equivalent per ton (y axis) of formation fluids from the formation versus temperature ("T") of the heated formation in degrees Celsius (x axis).
Desorption of inethane and vaporization of water occurs during stage 1 heating. Heating the formation through stage 1 may be performed as quickly as possible. When the formation is initially heated, hydrocarbons in the formation desorb adsorbed methane. The desorbed methane may be produced from the formation. If the formation is heated further, water in the formation is vaporized. Water may occupy, in some formations, between 10% and 50% of the pore volume in the formation. In other formations, water occupies larger or smaller portions of the pore volume. Water typically is vaporized in the formation between 160 C and 285 C
at pressures of 600 kPa absolute to 7000 kPa absolute. In some embodiments, the vaporized water produces wettability changes in the formation and/or increased formation pressure. The wettability changes and/or increased pressure may affect pyrolysis reactions or other reactions in the fonnation. In certain embodiments, the vaporized water is produced from the foi7nation. In other embodiments, the vaporized water is used for steam extraction and/or distillation in the formation or outside the formation. Reinoving the water from the formation and increasing the pore volume in the formation increases the storage space for hydrocarbons in the pore volume.
In certain embodiments, after stage 1 heating, the portion of the formation is heated further, such that the temperature in the portion of the formation reaches (at least) an initial pyrolyzation temperature (such as a temperature at the lower end of the temperature range shown as stage 2).
Hydrocarbons in the formation may be pyrolyzed tliroughout stage 2. A pyrolysis temperature range varies depending on the types of hydrocarbons in the formation. The pyrolysis temperature range may include temperatures between 250 C and 900 C. The pyrolysis temperature range for producing desired products may extend through only a portion of the total pyrolysis temperature range. In some embodiments, the pyrolysis temperature range for producing desired products may include temperatures between 250 C and 400 C, temperatures between 250 C and 350 C, or temperatures between 325 C and 400 C. If the teinperature of hydrocarbons in the formation is slowly raised through the temperature range from 250 C to 400 C, production of pyrolysis products may be substantially complete when the temperature approaches 400 C. Heating the formation with a plurality of heat sources may establish thermal gradients around the heat sources that slowly raise the temperature of hydrocarbons in the formation through the pyrolysis temperature range.
In some in situ conversion embodiments, a portion of the formation is heated to the desired temperature instead of slowly heating the temperature through the pyrolysis temperature range. In some embodiments, the desired temperature is 300 C. In some embodiments, the desired temperature is 325 C. In some embodiments, the desired temperature is 350 C. Other temperatures may be selected as the desired temperature. Superposition of heat from heat sources allows the desired temperature to be relatively quickly and efficiently established in the formation. Energy input into the formation from the heat sources may be adjusted to maintain the temperature in the formation at the desired temperature. The heated portion of the formation is maintained substantially at the desired temperature until pyrolysis declines such that production of desired formation fluids from the formation becomes uneconomical. Parts of the formation that are subjected to pyrolysis may include regions brought into the pyrolysis temperature range by heat transfer from only one heat source.
In certain embodiments, formation fluids including pyrolyzation fluids are produced from the formation. As the temperature of the formation increases, the amount of condensable hydrocarbons in the produced formation fluid may decrease. At high temperatures, the formation may produce mostly methane and/or hydrogen. If the formation is heated throughout an entire pyrolysis range, the formation may produce only small amounts of hydrogen towards an upper limit of the pyrolysis range.
After most of the available hydrogen is depleted, a minimal ainount of fluid production will occur from the formation.
After pyrolysis of hydrocarbons, a large amount of carbon and some hydrogen may still be present in the heated portion of the formation. Some carbon remaining in the heated portion of the formation may be produced from the fonnation in the form of synthesis gas. Synthesis gas generation may take place during stage 3 heating depicted in FIG. 1. Stage 3 may include heating the heated portion of the formation to a temperature sufficient to allow synthesis gas generation. Synthesis gas may be produced in a temperature range from 400 C
to 1200 C, 500 C to 1100 C, or 550 C to 1000 C. The temperature of the heated portion of the formation when the synthesis gas generating fluid is introduced to the forma.tion determines the composition of synthesis gas produced in the formation. Generated synthesis gas may be removed from the formation tlirough one or more production wells.
FIG. 2 depicts a schematic view of an embodiment of a portion of the in situ conversion system for treating the formation that contains hydrocarbons. Heat sources 100 are placed in at least a portion of the formation. Heat sources 100 may include electric heaters such as insulated conductors, conductor-in-conduit heaters, surface buiners, flameless distributed combustors, and/or natural distributed combustors. Heat sources 100 may also include other types of heaters. Heat sources 100 provide heat to at least a portion of the formation to heat hydrocarbons in the formation. Energy may be supplied to heat sources 100 through supply lines 102.
Supply lines 102 may be structurally different depending on the type of heat source or heat sources used to heat the formation. Supply lines 102 for heat sources may transinit electricity for electric heaters, may transport fuel for combustors, or may transport heat exchange fluid that is circulated in the formation.
Production wells 104 are used to remove formation fluid from the formation.
Formation fluid produced from production wells 104 may be transported through collection piping 106 to treatment facilities 108. Formation fluids may also be produced from heat sources 100. For example, fluid may be produced from heat sources 100 to control pressure in the formation adjacent to the heat sources. Fluid produced from heat sources 100 may be transported through tubing or piping to collection piping 106 or the produced fluid may be transported through tubing or piping directly to treatment facilities 108.
Treatment facilities 108 may include separation units, reaction units, upgrading units, fuel cells, turbines, storage vessels, and/or other systems and units for processing produced formation fluids.
The in situ conversion system for treating hydrocarbons may include barrier wells 110. Barrier wells are used to form a barrier around a treatment area. The barrier inhibits fluid flow into and/or out of the treatment area. Barrier wells include, but are not limited to, dewatering wells, vacuum wells, capture wells, injection wells, grout wells, freeze wells, or combinations thereof. In some embodiments, barrier wells 110 are dewatering wells. Dewatering wells may remove liquid water and/or inhibit liquid water from entering a portion of the formation to be heated, or to the formation being heated. In the embodiment depicted in FIG. 2, the dewatering wells are shown extending only along one side of heat sources 100, but dewatering wells typically encircle all heat sources 100 used, or to be used, to heat the formation.
As shown in FIG. 2, in addition to heat sources 100, one or more production wells 104 are placed in the formation. Formation fluids may be produced through production well 104. In sonie embodiments, production well 104 includes a heat source. The heat source in the production well may heat one or more portions of the formation at or near the production well and allow for vapor phase removal of formation fluids. The need for high temperature pumping of liquids from the production well may be reduced or eliminated. Avoiding or limiting high temperature pumping of liquids may significantly decrease production costs. Providing heating at or through the production well may: (1) inhibit condensation and/or refluxing of production fluid when such production fluid is moving in the production well proximate the overburden, (2) increase heat input into the formation, and/or (3) increase formation permeability at or proximate the production well. In some in situ conversion process embodiments, an amount of heat supplied to the formation from a production well per meter of the production well is less than the amount of heat applied to the fonnation from a heat source that heats the formation per meter of the heat source.
In some in situ conversion process embodiments, increased pressure due to fluid generation may be maintained in the heated portion of the formation. Maintaining increased pressure in the formation may inhibit formation subsidence during in situ conversion. Increased formation pressure may promote generation of high quality products during pyrolysis. Increased formation pressure may facilitate vapor phase production of fluids from the formation. Vapor phase production may allow for a reduction in size of collection conduits used to transport fluids produced from the formation. Increased formation pressure may reduce or eliminate the need to compress formation fluids at the surface to transport the fluids in collection conduits to treatment facilities.
Increased pressure in the formation may also be maintained to produce more and/or improved formation fluids. In certain in situ conversion process embodiments, significant amounts of the hydrocarbon fluids produced from the formation may be non-condensable hydrocarbons.
Pressure may be selectively increased and/or maintained in the formation to promote formation of smaller chain hydrocarbons in the formation. Producing small chain hydrocarbons in the formation may allow more non-condensable hydrocarbons to be produced from the formation. The condensable hydrocarbons produced from the formation at higher pressure may be of a higher quality as assessed by API gravity than condensable hydrocarbons produced from the formation at a lower pressure. In certain embodiments, the mixture produced from the formation includes condensable hydrocarbons having an API gravity of at least 25 or at least 30.
High pressure may be maintained in the heated portion of the formation to inhibit production of formation fluids with coinponents that have carbon numbers of 25 or greater.
Maintaining increased pressure in the heated portion of the formation may surprisingly allow for production of large quantities of hydrocarbons of increased quality. Higher pressures may inhibit vaporization of higher molecular weight hydrocarbons.
Inhibiting vaporization of higher molecular weight hydrocarbons may result in higher molecular weight hydrocarbons remaining in the formation. Higher molecular weight hydrocarbons may interact with lower molecular weight hydrocarbons in the formation to vaporize the lower molecular weight hydrocarbons.
Vaporized hydrocarbons may be more readily transported through the formation.
In certain embodiments, a "temperature limited heater" is used to provide heat to the formation. The temperature limited heater is a heater that regulates heat output (for example, reduces heat output) above a specified temperature without the use of external controls such as temperature controllers, power regulators, rectifiers or other devices.
Temperature limited heaters may be in configurations and/or may include materials that provide automatic temperature limiting properties for the heater at certain temperatures. In certain embodiments, ferromagnetic materials are used in temperature limited heaters. Ferromagnetic material may self-limit temperature at or near the Curie temperature of the inaterial to provide a reduced amount of heat at or near the Curie temperature when an time-varying current is applied to the material. In certain embodiments, the ferromagnetic material self-limits temperature of the temperature limited heater at a selected temperature that is approximately the Curie temperature. In certain embodiments, the selected teinperature is within about 35 C, within about 25 C, within about 20 C, or within about 10 C of the Curie teinperature. In certain embodiments, ferromagnetic materials are coupled with other materials (for example, highly conductive materials, high strength materials, corrosion resistant materials, or combinations thereof) to provide various electrical and/or mechanical properties. Some parts of the temperature limited heater may have a lower resistance (caused by different geometries and/or by using different ferromagnetic and/or non-ferromagnetic materials) than other parts of the temperature limited heater. Having parts of the temperature limited heater with various materials and/or diinensions allows for tailoring the desired heat output from each part of the heater.
Temperature limited heaters may be more reliable than other heaters.
Temperature limited heaters may be less apt to break down or fail due to hot spots in the formation. In some embodiments, temperature limited heaters allow for substantially uniform heating of the formation. In some embodiments, temperature limited heaters are able to heat the formation more efficiently by operating at a higher average heat output along the entire length of the heater. The temperature limited heater operates at the higher average heat output along the entire length of the heater because power to the heater does not have to be reduced to the entire heater, as is the case with typical constant wattage heaters, if a temperature along any point of the heater exceeds, or is about to exceed, a maximum operating temperature of the heater. Heat output from portions of a temperature limited heater approaching a Curie temperature of the heater automatically reduces without controlled adjustment of current applied to the heater. The heat output automatically reduces due to changes in electrical properties (for example, electrical resistance) of portions of the temperature limited heater.
Thus, more power is supplied by the temperature limited heater during a greater portion of a heating process.
In certain embodiments, the system including temperature limited heaters initially provides a first heat output and then provides a reduced (second heat output) heat output, near, at, or above the Curie temperature of an electrically resistive portion of the heater when the temperature limited heater is energized by a time-varying current. The first heat output is the heat output at temperatures below which the temperature limited heater begins to self-limit. In some embodiments, the first heat output is the heat output at a temperature 50 C, 75 C, 100 C, or 125 C below the Curie temperature of the ferromagnetic material in the temperature limited heater.
The temperature limited heater may be energized by time-varying current (alternating current or modulated direct current) supplied at the wellhead. The wellhead may include a power source and other components (for example, modulation components, transformers, and/or capacitors) used in supplying power to the temperature limited heater. The temperature limited heater may be one of many heaters used to heat a portion of the formation.
In certain embodiments, the temperature limited heater includes a conductor that operates as a skin effect or proximity effect heater when time-varying current is applied to the conductor. The skin effect limits the depth of current penetration into the interior of the conductor. For ferromagnetic materials, the skin effect is dominated by the magnetic permeability of the conductor. The relative magnetic permeability of ferromagnetic materials is typically between 10 and 1000 (for example, the relative magnetic permeability of ferromagnetic materials is typically at least 10 and may be at least 50, 100, 500, 1000 or greater). As the temperature of the ferromagnetic material is raised above the Curie temperature and/or as the applied electrical current is increased, the magnetic permeability of the ferromagnetic material decreases substantially and the skin depth expands rapidly (for example, the skin depth expands as the inverse square root of the magnetic permeability). The reduction in magnetic permeability results in a decrease in the AC or modulated DC resistance of the conductor near, at, or above the Curie temperature and/or as the applied electrical current is increased. When the temperature limited heater is powered by a substantially constant current source, portions of the heater that approach, reach, or are above the Curie temperature may have reduced heat dissipation. Sections of the temperature limited heater that are not at or near the Curie temperature may be dominated by skin effect heating that allows the heater to have high heat dissipation due to a higher resistive load.
An advantage of using the temperature liinited heater to heat hydrocarbons in the formation is that the conductor is chosen to have a Curie temperature in a desired range of temperature operation. Operation within the desired operating temperature range allows substantial heat injection into the formation while maintaining the temperature of the temperature limited heater, and other equipment, below design limit temperatures.
Design limit temperatures are temperatures at which properties such as corrosion, creep, and/or deformation are adversely affected. The temperature limiting properties of the temperature limited heater inhibits overheating or burnout of the heater adjacent to low thermal conductivity "hot spots" in the formation. In some embodiments, the temperature limited heater is able to lower or control heat output and/or withstand heat at temperatures above 25 C, 37 C, 100 C, 250 C, 500 C, 700 C, 800 C, 900 C, or higher up to 1500 C, depending on the materials used in the heater.
The temperature limited heater allows for more heat injection into the formation than constant wattage heaters because the energy input into the temperature limited heater does not have to be limited to accommodate low thermal conductivity regions adjacent to the heater. For example, in Green River oil shale there is a difference of at least 50% in the thermal conductivity of the lowest richness oil shale layers and the highest richness oil shale layers. When heating such a formation, substantially more heat is transferred to the formation with the temperature limited heater than with the conventional heater that is limited by the temperature at low thermal conductivity layers. The heat output along the entire length of the conventional heater needs to accommodate the low thermal conductivity layers so that the heater does not overheat at the low thermal conductivity layers and burn out. The heat output adjacent to the low thermal conductivity layers that are at high temperature will reduce for the temperature limited heater, but the remaining portions of the teinperature limited heater that are not at high temperature will still provide high heat output. Because heaters for heating hydrocarbon formations typically have long lengths (for example, at least 10 m, 100 m, 300 m, 1 km or more up to 10 km), the majority of the length of the teinperature limited heater may be operating below the Curie temperature, while only a few portions are at or near the Curie temperature of the temperature limited heater.
The use of temperature limited heaters allows for efficient transfer of heat to the formation. Efficient transfer of heat allows for reduction in time needed to heat the formation to a desired temperature. For example, in Green River oil shale, pyrolysis typically requires 9.5 years to 10 years of heating when using a 12 m heater well spacing with conventional constant wattage heaters. For the same heater spacing, temperature limited heaters may allow a larger average heat output while maintaining heater equipment temperatures below equipment design limit temperatures. Pyrolysis in the formation may occur at an earlier time with the larger average heat output provided by temperature limited heaters than the lower average heat output provided by constant wattage heaters. For example, in Green River oil shale, pyrolysis may occur in 5 years using temperature limited heaters with a 12 m heater well spacing. Temperature limited heaters counteract hot spots due to inaccurate well spacing or drilling where heater wells come too close together. In certain embodiments, temperature limited heaters allow for increased power output over time for heater wells that have been spaced too far apart, or limit power output for heater wells that are spaced too close together.
The ferromagnetic alloy or ferromagnetic alloys used in the temperature limited heater determine the Curie temperature of the heater. Curie temperature data for various metals is listed in "American Institute of Physics Handbook," Second Edition, McGraw-Hill, pages 5-170 tlirough 5-176.
Ferromagnetic conductors may include one or more of the ferromagnetic elements (iron, cobalt, and nickel) and/or alloys of these elements. In some einbodiments, ferromagnetic conductors include iron-cliromium alloys that contain tungsten (for example, HCM12A and SAVE12 (Sumitoino Metals Co., Japan) and/or iron alloys that contain chromium (for example, Fe-Cr alloys, Fe-Cr-W alloys, Fe-Cr-V alloys, Fe-Cr-Nb alloys). Of the three main ferromagnetic eleinents, iron has a Curie temperature of approximately 770 C; cobalt has a Curie temperature of approximately 1131 C; and nickel has a Curie temperature of approximately 358 C. An iron-cobalt alloy has a Curie temperature higher than the Curie temperature of iron. For example, an iron alloy with 2%
cobalt has a Curie temperature of approximately 800 C; an iron alloy with 12% cobalt has a Curie temperature of approximately 900 C; and an iron alloy with 20% cobalt has a Curie temperature of approximately 950 C. An iron-nickel alloy has a Curie temperature lower than the Curie temperature of iron. For example, an iron alloy with 20% nickel has a Curie temperature of approximately 720 C, and an iron alloy with 60% nickel has a Curie temperature of approxiunately 560 C.
Some non-ferromagnetic elements used as alloys raise the Curie temperature of iron. For example, an iron alloy with 5.9% vanadium has a Curie temperature of approximately 815 C.
Other non-ferromagnetic elements (for example, carbon, aluminum, copper, silicon, and/or chromium) may be alloyed with iron or other ferromagnetic inaterials to lower the Curie temperature. Non-ferromagnetic materials that raise the Curie temperature may be combined with non-ferromagnetic materials that lower the Curie temperature and alloyed with iron or other ferromagnetic materials to produce a material with a desired Curie temperature and other desired physical and/or chemical properties. In some embodiments, the Curie temperature material is a ferrite such as NiFeZO4. In other embodiments, the Curie temperature material is a binary compound such as FeNi3 or Fe3A1.

Certain embodiments of temperature limited heaters may include more than one ferromagnetic material. Such embodiments are within the scope of embodiments described herein if any conditions described herein apply to at least one of the ferromagnetic materials in the temperature limited heater.
Ferromagnetic properties generally decay as the Curie temperature is approached. The "Handbook of Electrical Heating for Industry" by C. James Erickson (IEEE Press, 1995) shows a typical curve for 1% carbon steel (i.e., steel with 1% carbon by weight). The loss of magnetic permeability starts at temperatures above 650 C and tends to be complete when temperatures exceed 730 C. Thus, the self-limiting temperature may be somewhat below an actual Curie temperature of the ferromagnetic conductor. The skin depth for current flow in 1% carbon steel is 0.132 cm at room temperature and increases to 0.445 cm at 720 C. From 720 C to 730 C, the skin depth sharply increases to over 2.5 cm. Thus, a temperature liinited heater embodiment using 1%
carbon steel begins to self-limit between 650 C and 730 C.
Skin depth generally defines an effective penetration depth of tiine-varying current into a conductive material. In general, current density decreases exponentially with distance from an outer surface to a center along a radius of a conductor. The depth at which the current density is approximately lle of the surface current density is called the skin depth. For a solid cylindrical rod with a diameter much greater than the penetration depth, or for hollow cylinders with a wall thickness exceeding the penetration depth, the skin depth, S, is:
(1) S = 1981.5* (pl( *f))Ii2;
in which: S= skin depth in inches;
p = resistivity at operating temperature (ohm-cm);
= relative magnetic permeability; and f = frequency (Hz).
EQN. 1 is obtained from "Handbook of Electrical Heating for Industry" by C.
James Erickson (IEEE
Press, 1995). For most metals, resistivity (p) increases with temperature. The relative magnetic permeability generally varies with temperature and with current. Additional equations may be used to assess the variance of magnetic permeability and/or skin depth on both temperature and/or current.
The dependence of on current arises from the dependence of on the magnetic field.
Materials used in the temperature limited heater may be selected to provide a desired turndown ratio.
Turndown ratios of at least 2:1, 3:1, 4:1, 5:1, 10:1, 30:1, or 50:1 may be selected for temperature limited heaters.
Larger turndown ratios may also be used. The selected turndown ratio depends on a number of factors including, but not limited to, the type of formation in which the temperature limited heater is located and/or a temperature limit of materials used in the wellbore. In some embodiments, the turndown ratio is increased by coupling additional copper or another good electrical conductor to the ferromagnetic material (for example, adding copper to lower the resistance above the Curie temperature).
The temperature limited heater may provide a minimum heat output (power output) below the Curie temperature of the heater. In certain embodiments, the minimum heat output is at least 400 W/m, 600 W/m, 700 W/m, 800 W/m, or higher. The temperature limited heater may reduce the amount of heat output by a section of the heater when the temperature of the section of the heater approaches or is above the Curie temperature. The reduced amount of heat may be substantially less than the heat output below the Curie temperature. In some embodiinents, the reduced amount of heat is at most 400 W/m, 200 W/m, or may approach 100 W/m, or less.

In certain embodiments, the temperature limited heater operates substantially independently of the thermal load on the heater in a certain operating temperature range.
"Thermalload" is the rate that heat is transferred from a heating system to its surroundings. It is to be understood that the thermal load may vary with temperature of the surroundings and/or the thermal conductivity of the surroundings. In an embodiment, the temperature limited heater operates at or above the Curie temperature of the temperature limited heater such that the operating temperature of the heater increases at most by 3 C, 2 C, 1.5 C, 1 C, or 0.5 C for a decrease in thermal load of 1 W/m proximate to a portion of the heater. In certain embodiments, the temperature limited heater operates in such a manner at a relatively constant current.
The AC or modulated DC resistance and/or the heat output of the temperature limited heater may decrease as the temperature approaches the Curie temperature and decrease sharply near or above the Curie temperature due to the Curie effect. In certain embodiments, the value of the electrical resistance or heat output above or near the Curie temperature is at most one-half of the value of electrical resistance or heat output at a certain point below the Curie temperature. In some embodiments, the heat output above or near the Curie temperature is at most 40%, 30%, 20% or less of the heat output at a certain point below the Curie temperature (for example, 30 C below the Curie teinperature, 40 C below the Curie temperature, 50 C below the Curie temperature, or 100 C below the Curie temperature). In certain embodiments, the electrical resistance above or near the Curie temperature decreases to 80%, 70%, 60%, or 50% of the electrical resistance at a certain point below the Curie temperature (for example, 30 C below the Curie temperature, 40 C below the Curie temperature, 50 C below the Curie temperature, or 100 C below the Curie temperature).
In some embodiments, AC frequency is adjusted to change the skin depth of the ferromagnetic material. For exainple, the skin depth of 1% carbon steel at room temperature is 0.132 cm at 60 Hz, 0.0762 cm at 180 Hz, and 0.046 cm at 440 Hz. Since heater diameter is typically larger than twice the skin depth, using a higher frequency (and thus a heater with a smaller diameter) reduces equipment costs. For a fixed geometry, the higher frequency results in a higher turndown ratio. The turndown ratio at a higher frequency is calculated by multiplying the turndown ratio at a lower fiequency by the square root of the higher frequency divided by the lower frequency. In some embodiments, a frequency between 100 Hz and 1000 Hz, between 140 Hz and 200 Hz, or between 400 Hz and 600 Hz is used (for example, 180 Hz, 540 Hz, or 720 Hz). In some embodiments, high frequencies may be used. The frequencies may be greater than 1000 Hz.
To maintain a substantially constant skin depth until the Curie temperature of the temperature limited heater is reached, the heater may be operated at a lower frequency when the heater is cold and operated at a higher frequency when the heater is hot. Line frequency heating is generally favorable, however, because there is less need for expensive components such as power supplies, transformers, or current modulators that alter frequency. Line frequency is the frequency of a general supply of current.
Line frequency is typically 60 Hz, but may be 50 Hz or another frequency depending on the source for the supply of the current. Higher frequencies may be produced using commercially available equipment such as solid state variable frequency power supplies. Transformers that convert tliree-phase power to single-phase power with three times the frequency are commercially available. For example, high voltage three-phase power at 60 Hz may be transformed to single-phase power at 180 Hz and at a lower voltage. Such transformers are less expensive and more energy efficient than solid state variable frequency power supplies. In certain embodiments, transformers that convert three-phase power to single-phase power are used to increase the frequency of power supplied to a heater.
In certain embodiments, modulated DC (for exainple, chopped DC, waveform modulated DC, or cycled DC) may be used for providing electrical power to the temperature liinited heater. A DC modulator or DC chopper may be coupled to a DC power supply to provide an output of modulated direct current. In some embodiments, the DC power supply may include means for modulating DC. One example of a DC modulator is a DC-to-DC converter system. DC-to-DC converter systems are generally known in the art. DC is typically modulated or chopped into a desired waveform. Waveforms for DC modulation include, but are not limited to, square-wave, sinusoidal, deformed sinusoidal, deformed square-wave, triangular, and other regular or irregular waveforms.
The modulated DC waveform generally defines the frequency of the modulated DC.
Thus, the modulated DC waveform may be selected to provide a desired modulated DC
frequency. The shape and/or the rate of modulation (such as the rate of chopping) of the modulated DC waveform may be varied to vary the modulated DC frequency. DC may be modulated at frequencies that are higher than generally available AC
frequencies. For example, modulated DC may be provided at frequencies of at least 1000 Hz. Increasing the frequency of supplied current to higher values advantageously increases the turndown ratio of the temperature limited heater.
In certain embodiments, the modulated DC waveform is adjusted or altered to vary the modulated DC
frequency. The DC modulator may be able to adjust or alter the modulated DC
waveform at any time during use of the temperature limited heater and at high currents or voltages. Thus, modulated DC provided to a temperahue limited heater is not limited to a single frequency or even a small set of frequency values.
Waveform selection using the DC modulator typically allows for a wide range of modulated DC frequencies and for discrete control of the modulated DC frequency. Thus, the modulated DC
frequency is more easily set at a distinct value, whereas AC frequency is generally limited to multiples of the line frequency. Discrete control of the modulated DC frequency allows for more selective control over the turndown ratio of a temperature limited heater. Being able to selectively control a turndown ratio of a temperature limited heater allows for a broader range of materials to be used in designing and constructing a teinperature limited heater.
In certain embodiments, the temperature limited heater includes an inner conductor inside an outer conductor. The inner conductor and the outer conductor are radially disposed about a central axis. The inner and outer conductors may be separated by an insulation layer. In certain embodiments, the inner and outer conductors are coupled at the bottom of the temperature limited heater.
Electrical current may flow into the temperature limited heater through the inner conductor and return through the outer conductor. One or both conductors may include ferromagnetic material.
An insulation layer may coinprise an electrically insulating ceramic with high thermal conductivity, such as magnesium oxide, aluminum oxide, silicon dioxide, beryllium oxide, boron nitride, silicon nitride or combinations thereof. The insulating layer may be a compacted powder (for example, compacted ceramic powder). Compaction may improve thermal conductivity and provide better insulation resistance. For low temperature applications, polymer insulation made froni, for example, fluoropolymers, polyimides, polyamides, and/or polyethylenes, may be used. In some embodiments, the polymer insulation is made of perfluoroalkoxy (PFA) or polyetheretherketone (PEEKTM). The insulating layer may be chosen to be substantially infrared transparent to aid heat transfer from the inner conductor to the outer conductor. In an embodiment, the insulating layer is transparent quartz sand. The insulation layer may be air or a non-reactive gas such as helium, nitrogen, or sulfur hexafluoride. If the insulation layer is air or a non-reactive gas, there may be insulating spacers designed to inhibit electrical contact between the inner conductor and the outer conductor. The insulating spacers may be made of, for example, high purity aluminum oxide or another thermally conducting, electrically insulating material such as silicon nitride. The insulating spacers may be a fibrous ceramic material such as NextelTM 312, mica tape, or glass fiber. Ceramic material may be made of alumina, alumina-silicate, alumina-borosilicate, silicon nitride, or other materials.
The insulation layer may be flexible and/or substantially deformation tolerant. For example, if the insulation layer is a solid or compacted material that substantially fills the space between the inner and outer conductors, the temperature limited heater may be flexible and/or substantially deformation tolerant. Forces on the outer conductor can be transmitted through the insulation layer to the solid inner conductor, which may resist crushing. Such a temperature limited heater may be bent, dog-legged, and spiraled without causing the outer conductor and the inner conductor to electrically short to each other.
Deformation tolerance may be important if the wellbore is likely to undergo substantial deformation during heating of the formation.
In certain embodiments described herein, temperature limited heaters are dimensioned to operate at a frequency of 60 Hz AC. It is to be understood that dimensions of the temperature limited heater may be adjusted from those described herein for the temperature limited heater to operate in a similar manner at other AC frequencies or with modulated DC. FIG. 3 depicts a cross-sectional representation of an embodiment of a temperature limited heater with an outer conductor having a ferromagnetic section and a non-ferromagnetic section. FIGS. 4 and 5 depict transverse cross-sectional views of the embodiment shown in FIG. 3. In one embodiment, ferromagnetic section 112 is used to provide heat to hydrocarbon layers in the formation. Non-ferromagnetic section 114 is used in the overburden of the formation. Non-ferromagnetic section 114 provides little or no heat to the overburden, thus inhibiting heat losses in the overburden and improving heater efficiency.
Ferromagnetic section 112 includes a ferromagnetic material such as 409 stainless steel or 410 stainless steel.
409 stainless steel is readily available as strip material. Ferromagnetic section 112 has a thickness of 0.3 cm.
Non-ferromagnetic section 114 is copper with a thickness of 0.3 cm. Inner conductor 116 is copper. Inner conductor 116 has a diameter of 0.9 cm. Electrical insulator 118 is silicon nitride, boron nitride, magnesiuin oxide powder, or another suitable insulator material. Electrical insulator 118 has a thickness of 0.1 cm to 0.3 cm.
FIG. 6 depicts a cross-sectional representation of an embodiment of a temperature limited heater with an outer conductor having a ferromagnetic section and a non-ferromagnetic section placed inside a sheath.
FIGS. 7, 8, and 9 depict transverse cross-sectional views of the embodiment shown in FIG. 6. Ferromagnetic section 112 is 410 stainless steel with a thickness of 0.6 cm. Non-ferromagnetic section 114 is copper with a thickness of 0.6 cm. Imier conductor 116 is copper with a diameter of 0.9 cm.
Outer conductor 120 includes ferromagnetic material. Outer conductor 120 provides some heat in the overburden section of the heater.
Providing some heat in the overburden inhibits condensation or refluxing of fluids in the overburden. Outer conductor 120 is 409, 410, or 446 stainless steel with an outer diameter of 3.0 cm and a thickness of 0.6 cm.
Electrical insulator 118 includes compacted is magnesium oxide powder with a thickness of 0.3 cm. In some embodiments, electrical insulator 118 is includes silicon nitride, boron nitride, or hexagonal type boron nitride.

Conductive section 122 may couple inner conductor 116 with feiTomagnetic section 112 and/or outer conductor 120.
FIG. 10 depicts a cross-sectional representation of an embodiment of a temperature limited heater with an outer conductor. The outer conductor includes a ferromagnetic section and a non-ferromagnetic section. The heater is placed in a corrosion resistant jacket. A conductive layer is placed between the outer conductor and the jacket. FIGS. 11 and 12 depict transverse cross-sectional views of the embodiment shown in FIG. 10.
Ferromagnetic section 112 is 409, 410, or 446 stainless steel with a thickness of 0.9 cm. Non-ferromagnetic section 114 is copper with a thickness of 0.9 cm. Conductive layer 124 is a copper layer. Ferromagnetic section 112, non-ferromagnetic section 114, and conductive layer 124 are placed in jacket 126. Jacket 126 is 304 or 347H stainless steel with a thickness of 0.1 cm. Electrical insulator 118 includes compacted is silicon nitride, boron nitride, or magnesium oxide powder with a thickness of 0.1 to 0.3 cm.
Inner conductor 116 is copper with a diameter of 1.0 cm.
In an embodiment, ferromagnetic section 112 is 446 stainless steel with a thickness of 0.9 cm. Jacket 126 is 410 stainless steel with a thickness of 0.6 cm. 410 stainless steel has a higher Curie temperature than 446 stainless steel. Such a temperature limited heater may "contain" current such that the current does not easily flow from the heater to the surrounding formation and/or to any surrounding water (for example, brine, groundwater, or formation water). In this embodiment, current flows through ferromagnetic section 112 until the Curie temperature of the ferromagnetic section is reached. After the Curie teinperature of ferromagnetic section 112 is reached, current flows through conductive layer 124. The ferromagnetic properties ofjacket 126 (410 stainless steel) inhibit the current from flowing outside the jacket and "contain" the current. Jacket 126 may also have a thickness that provides strength to the temperature limited heater.
FIG. 13 depicts a cross-sectional representation of an embodiment of a temperature limited heater. The heating section of the temperature limited heater includes non-ferromagnetic inner conductors and a ferromagnetic outer conductor. The overburden section of the temperature limited heater includes a non-ferromagnetic outer conductor. FIGS. 14, 15, and 16 depict transverse cross-sectional views of the embodiment shown in FIG. 13. Inner conductor 116 is copper with a diameter of 1.0 cm.
Electrical insulator 118 is placed between inner conductor 116 and conductive layer 124. Electrical insulator 118 includes compacted silicon nitride, boron nitride, or magnesium oxide powder with a thickness of 0.1 cm to 0.3 cm. Conductive layer 124 is copper with a thickness of 0.1 cm. Insulation layer 128 is in the annulus outside of conductive layer 124. The thickness of the annulus may be 0.3 cm. In some embodiments, insulation layer 128 is quartz sand.
Heating section 130 may provide heat to one or more hydrocarbon layers in the formation. Heating section 130 includes ferromagnetic material such as 409 stainless steel or 410 stainless steel. Heating section 130 has a thickness of 0.9 cm. Endcap 132 is coupled to an end of heating section 130. Endcap 132 electrically couples heating section 130 to imier conductor 116 and/or conductive layer 124. Endcap 132 is 304 stainless steel. Heating section 130 is coupled to overburden section 134. Overburden section 134 includes carbon steel and/or other suitable support materials. Overburden section 134 has a thickness of 0.6 cm. Overburden section 134 is lined with conductive layer 135. Conductive layer 135 is copper with a thickness of 0.3 cm.
FIG. 17A and FIG. 17B depict cross-sectional representations of an embodiment of a temperature limited heater with a ferromagnetic inner conductor. hmer conductor 116 is a 1" Schedule XXS 446 stainless steel pipe. In some embodiments, inner conductor 116 includes 409 stainless steel, 410 stainless steel, Invar 36, alloy 42-6, or other ferromagnetic materials. Inner conductor 116 has a diameter of 2.5 cm. Electrical insulator 118 includes compacted silicon nitride, boron nitride, or magnesium oxide powders; or polymers, Nextel ceramic fiber, mica, or glass fibersis silicon nitride, boron nitride, magnesium oxide (for example, magnesium oxide powder), polymers, Nextel ceramic fiber, mica, or glass fibers. Outer conductor 120 is copper or any other non-ferromagnetic material such as aluminum. Outer conductor 120 is coupled to jacket 126. Jacket 126 is 304H, 316H, or 347H stainless steel. In this embodiment, a majority of the heat is produced in inner conductor 116.
FIG. 18A and FIG. 18B depict cross-sectional representations of an embodiment of a temperature limited heater with a ferromagnetic inner conductor and a non-ferromagnetic core. Inner conductor 116 may be made of 446 stainless steel, 409 stainless steel, 410 stainless steel, carbon steel, Armco ingot iron, iron-cobalt alloys, or other ferromagnetic materials. Core 136 may be tightly bonded inside inner conductor 116. Core 136 is copper or other non-ferromagnetic material. In certain enzbodiments, core 136 is inserted as a tight fit inside inner conductor 116 before a drawing operation. In some embodiments, core 136 and inner conductor 116 are coextrusion bonded. Outer conductor 120 is 347H stainless steel. A drawing or rolling operation to compact electrical insulator 118 (for example, compacted silicon nitride, boron nitride, or rna.gnesium oxide powder) may ensure good electrical contact between inner conductor 116 and core 136. In this embodiment, heat is produced primarily in iimer conductor 116 until the Curie temperature is approached.
Resistance then decreases sharply as current penetrates core 136.
In some embodiments, a conductor (for example, the inner conductor, the outer conductor, or the ferromagnetic conductor) is a composite conductor that includes two or more different materials. In certain embodiments, the composite conductor includes two or more ferromagnetic materials. In some embodiments, the composite ferromagnetic conductor includes two or more radially disposed materials. In certain embodiments, the composite conductor includes a ferromagnetic conductor and a non-ferromagnetic conductor.
In some embodiments, the composite conductor includes a ferromagnetic conductor placed over a non-ferromagnetic core. Two or more materials may be used to obtain a relatively flat electrical resistivity versus temperature profile in a temperature region below the Curie temperature and/or a sharp decrease (a relatively high turndown ratio) in the electrical resistivity at or near the Curie temperature. In some cases, two or more materials are used to provide niore than one Curie temperature for the temperature limited heater.
In certain embodiments, the composite electrical conductor is used as the conductor in a conductor-in-conduit heater. For example, the composite electrical conductor may be used as conductor 138 in FIGS. 19 and 20.
FIG. 19 depicts a cross-sectional representation of an embodiment of a conductor-in-conduit heat source. Conductor 138 is disposed in conduit 140. Conductor 138 is a rod or conduit of electrically conductive material. Low resistance sections 142 is present at both ends of conductor 138 to generate less heating in these sections. Low resistance section 142 is formed by having a greater cross-sectional area of conductor 138 in that section, or the sections are made of material having less resistance. In certain embodiments, low resistance section 142 includes a low resistance conductor coupled to conductor 138.
Conduit 140 is made of an electrically conductive material. Conduit 140 is disposed in opening 144 in hydrocarbon layer 146. Opening 144 has a diameter able to accommodate conduit 140.

Conductor 138 inay be centered in conduit 140 by centralizers 148.
Centralizers 148 electrically isolate conductor 138 from conduit 140. Centralizers 148 inhibit movement and properly locate conductor 138 in conduit 140. Centralizers 148 are made of a ceramic material or a combination of ceramic and metallic materials. Centralizers 148 inhibit deformation of conductor 138 in conduit 140. Centralizers 148 are touching or spaced at intervals between approximately 0.1 m and approximately 3 m or more along conductor 138.
A second low resistance section 142 of conductor 138 may couple conductor 138 to wellhead 150, as depicted in FIG. 19. Electrical current may be applied to conductor 138 from power cable 152 through low resistance section 142 of conductor 138. Electrical current passes from conductor 138 through sliding coimector 154 to conduit 140. Conduit 140 may be electrically insulated fiom overburden casing 156 and from wellhead 150 to return electrical current to power cable 152. Heat may be generated in conductor 138 and conduit 140.
The generated heat may radiate in conduit 140 and opening 144 to heat at least a portion of hydrocarbon layer 146.
Overburden casing 156 may be disposed in overburden 158. Overburden casing 156 is, in some embodiments, surrounded by materials (for exainple, reinforcing material and/or cement) that inliibit heating of overburden 158. Low resistance section 142 of conductor 138 may be placed in overburden casing 156. Low resistance section 142 of conductor 138 is made of, for example, carbon steel.
Low resistance section 142 of conductor 138 may be centralized in overburden casing 156 using centralizers 148. Centralizers 148 are spaced at intervals of approximately 6 m to approxiinately 12 m or, for example, approximately 9 m along low resistance section 142 of conductor 138. In a heat source embodiment, low resistance section 142 of conductor 138 is coupled to conductor 138 by a weld or welds. In other heat source embodiments, low resistance sections are threaded, threaded and welded, or otherwise coupled to the conductor. Low resistance section 142 generates little and/or no heat in overburden casing 156. Packing 160 may be placed between overburden casing 156 and opening 144. Packing 160 may be used as a cap at the junction of overburden 158 and hydrocarbon layer 146 to allow filling of materials in the annulus between overburden casing 156 and opening 144. In some embodiments, packing 160 inliibits fluid from flowing from opening 144 to surface 162.
FIG. 20 depicts a cross-sectional representation of an embodiment of a removable conductor-in-conduit heat source. Conduit 140 is placed in opening 144 through overburden 158 such that a gap remains between the conduit and overburden casing 156. Fluids may be removed from opening 144 tlirough the gap between conduit 140 and overburden casing 156. Fluids may be removed from the gap tlirough conduit 164. Conduit 140 and components of the heat source included in the conduit that are coupled to wellhead 150 may be removed from opening 144 as a single unit. The heat source may be removed as a single unit to be repaired, replaced, and/or used in another portion of the formation.
In certain embodiments, the composite electrical conductor may be used as the conductor in the insulated conductor heater. FIG. 21A and FIG. 21B depict an embodiment of an insulated conductor heater.
Insulated conductor 166 includes core 136 and inner conductor 116. Core 136 and inner conductor 116 are located within insulator 118. Core 136, inner conductor 116, and insulator 118 are located inside outer conductor 120. Insulator 118 is silicon nitride, boron nitride, magnesium oxide, or another suitable electrical insulator. Outer conductor 120 is copper, steel, or any other electrical conductor.
In certain embodiments, insulator 118 is a powdered insulator. In some embodiments, insulator 118 is an insulator with a preformed shape such as preformed half-shells. A composite electrical conductor having core 136 and inner conductor 116 is placed inside the preformed insulator.
Outer conductor 120 is placed over insulator 118 by coupling (for exainple, by welding or brazing) one or more longitudinal strips of electrical conductor together to form the outer conductor. The longitudinal strips are placed over insulator 118 in a "cigarette wrap" method to couple the strips in a widthwise or radial direction (i.e., placing individual strips around the circumference of the insulator and coupling the individual strips to surround the insulator). The lengthwise ends of the cigarette wrapped strips may be coupled to lengthwise ends of other cigarette wrapped strips to couple the strips lengthwise along the insulated conductor.
In certain embodiments, centralizers (such as centralizers 148 depicted in FIGS. 19 and 20) are made of silicon nitride. In some embodiments, silicon nitride is gas pressure sintered reaction bonded silicon nitride.
Gas pressure sintered reaction bonded silicon nitride can be made by sintering the silicon nitride at 1800 C in a 10.3 MPa nitrogen atmosphere to inhibit degradation of the silicon nitride during sintering. One example of a gas pressure sintered reaction bonded silicon iiitride is obtained from Ceradyne, Inc. (Costa Mesa, Califoniia, U.S.A.) as Ceralloy 147-31N.
Gas pressure sintered reaction bonded silicon nitride may be ground to a fme fmish. The fine finish (which gives a very low surface porosity of the silicon nitride) allows the silicon nitride to slide easily along metal surfaces without picking up metal particles from the surfaces. Gas pressure sintered reaction bonded silicon nitride is a very dense material with high tensile strength, high flexural mechanical strength, and high thermal impact stress characteristics. Gas pressure sintered reaction bonded silicon nitride is an excellent liigh temperature electrical insulator. Gas pressure sintered reaction bonded silicon nitride has about the same leakage current at 900 C as alumina (A1203) at 760 C. Gas pressure sintered reaction bonded silicon nitride has a thermal conductivity of 25 watts per meter=K. The relatively high thermal conductivity promotes heat transfer away from the center conductor of a conductor-in-conduit heater.
Other types of silicon nitride such as, but not limited to, reaction-bonded silicon nitride or hot isostatically pressed silicon nitride may be used. Hot isostatic pressing includes sintering granular silicon nitride and additives at 100-200 MPa in nitrogen gas. Some silicon nitrides are made by sintering silicon nitride with yttrium oxide or cerium oxide to lower the sintering temperature so that the silicon nitride does not degrade (for example, by releasing nitrogen) during sintering. However, adding other material to the silicon nitride may increase the leakage current of the silicon nitride at elevated temperatures compared to purer forms of silicon nitride.
FIG. 22 depicts an embodiment of a conductor-in-conduit temperature limited heater. Conductor 138 is coupled to ferromagnetic conductor 168 (for example, clad, coextruded, press fit, drawn inside). In some embodiments, ferromagnetic conductor 168 is coextruded over conductor 138.
Ferromagnetic conductor 168 is coupled to the outside of conductor 138 so that current propagates only through the skin depth of the ferromagnetic conductor at room temperature. Ferromagnetic conductor 168 provides mechanical support for conductor 138 at elevated temperatures. Ferromagnetic conductor 168 is, for example, iron, iron alloy, or any other ferromagnetic material. In an embodiment, conductor 138 is copper and ferromagnetic conductor 168 is 446 stainless steel.
Conductor 138 and ferromagnetic conductor 168 are electrically coupled to conduit 140 with sliding connector 154. Conduit 140 is a non-ferromagnetic material such as, but not limited to, 347H stainless steel. In one embodiment, conduit 140 is a 1-'/2" Schedule 80 347H stainless steel pipe.
In another embodiment, conduit 140 is a Schedule XXH 347H stainless steel pipe. One or more centralizers 148 maintain the gap between conduit 140 and ferromagnetic conductor 168. In an embodiment, centralizer 148 is made of gas pressure sintered reaction bonded silicon nitride. Centralizer 148 may be held in position on ferromagnetic conductor 168 by one or more weld tabs located on the ferromagnetic conductor.
A temperature limited heater may be constructed in sections that are coupled (welded) together. The sections may be 10 m long or longer. Construction materials for each section are chosen to provide a selected heat output for different parts of the formation. For example, an oil shale formation may contain layers with highly variable richnesses. Providing selected amounts of heat to individual layers, or multiple layers with similar richnesses, improves heating efficiency of the formation and/or inhibits collapse of the wellbore. A
splice section may be formed between the sections, for example, by welding the inner conductors, filling the splice section with an insulator, and then welding the outer conductor.
Alternatively, the heater is formed from larger diameter tubulars and drawn down to a desired length and diameter. A
boron nitride, silicon nitride, magnesium oxide, or other type of insulation layer may be added by a weld-fill-draw method (starting from metal strip) or a fill-draw method (starting from tubulars) well known in the industry in the manufacture of mineral insulated heater cables. The assembly and filling can be done in a vertical or a horizontal orientation.
The fmal heater assembly may be spooled onto a large diameter spool (for example, 1 m, 2 m, 3 m, or more in diameter) and transported to a site of a formation for subsurface deployment.
Alternatively, the heater may be assembled on site in sections as the heater is lowered vertically into a wellbore.
A temperature limited heater may be a single-phase heater or a three-phase heater. In a three-phase heater embodiment, a heater has a delta or a wye configuration. Each of the three ferromagnetic conductors in a three-phase heater may be inside a separate sheath. A connection between conductors may be made at the bottom of the heater inside a splice section. The three conductors may remain insulated from the sheath inside the splice section.
FIG. 23 depicts an embodiment of a three-phase temperature limited heater with ferromagnetic inner conductors. Each leg 170 has iuuier conductor 116, core 136, and jacket 126.
Imier conductors 116 are ferritic stainless steel or 1% carbon steel. Inner conductors 116 have core 136. Core 136 may be copper. Each inner conductor 116 is coupled to its own jacket 126. Jacket 126 is a sheath made of a corrosion resistant material (such as 304H stainless steel). Electrical insulator 118 is placed between inner conductor 116 and jacket 126.
Inner conductor 116 is ferritic stainless steel or carbon steel with an outside diameter of 1.14 cm and a thickness of 0.445 cm. Core 136 is a copper core with a 0.25 cm diameter. Each leg 170 of the heater is coupled to terminal block 172. Terminal block 172 is filled with insulation material 174 and has an outer surface of stainless steel. Insulation material 174 is, in some embodiments, silicon nitride, boron nitride, magnesium oxide or other suitable electrically insulating material. Inner conductors 116 of legs 170 are coupled (welded) in terminal block 172. Jackets 126 of legs 170 are coupled (welded) to an outer surface of terminial block 172.
Terminal block 172 may include two halves coupled together around the coupled portions of legs 170.
In some three-phase heater embodiments, three ferromagnetic conductors are separated by an insulation layer inside a common outer metal sheath. The three conductors may be insulated from the sheath or the three conductors may be connected to the sheath at the bottom of the heater assembly. In another embodiment, a single outer sheath or three outer sheaths are ferromagnetic conductors and the inner conductors may be non-ferromagnetic (for example, aluminum, copper, or a highly conductive alloy).
Alternatively, each of the three non-ferromagnetic conductors are inside a separate ferromagnetic sheath, and a connection between the conductors is made at the bottom of the heater inside a splice section. The three conductors may remain insulated from the sheath inside the splice section.
FIG. 24 depicts an embodiment of a three-phase temperature limited heater with ferromagnetic inner conductors in a common jacket. Inner conductors 116 surround cores 136. Iimer conductors 116 are placed in electrical insulator 118. Inner conductors 116 and electrical insulator 118 are placed in a single jacket 126.
Jacket 126 is a sheath made of corrosion resistant material such as stainless steel. Jacket 126 has an outside diameter of between 2.5 cm and 5 cm (for example, 3.1 cm, 3.5 cm, or 3.8 cm).
Inner conductors 116 are coupled at or near the bottom of the heater at termination 176. Termination 176 is a welded termination of inner conductors 116. Inner conductors 116 may be coupled in a wye configuration.
Examples:
Non-restricting examples of temperature limited heaters and properties of temperature limited heaters are set forth below.
FIG. 25 depicts leakage current (mA)(milliamps) versus voltage (V) for alumina and silicon nitride centralizers at selected temperatures. Leakage current was measured between a conductor and a conduit of a 0.91 m conductor-in-conduit section with two centralizers. The conductor-in-conduit was placed horizontally in a furnace. Plot 178 depicts data for alumina centralizers at a temperature of 760 C. Plot 180 depicts data for alumina centralizers at a temperature of 815 C. Plot 182 depicts data for gas pressure sintered reaction bonded silicon nitride centralizers at a temperature of 760 C. Plot 184 depicts data for gas pressure sintered reaction bonded silicon nitride at a temperature of 871 C. FIG. 25 shows that the leakage current of alumina increases substantially from 760 C to 815 C while the leakage current of gas pressure sintered reaction bonded silicon nitride remains relatively low from 760 C to 871 C.
FIG. 26 depicts leakage current (inA) versus temperature ( C) for two different types of silicon nitride.
Plot 186 depicts leakage current versus temperature for highly polished, gas pressure sintered reaction bonded silicon nitride. Plot 188 depicts leakage current versus temperature for doped densified silicon nitride. FIG. 26 shows the improved leakage current versus temperature characteristics of gas pressure sintered reaction bonded silicon nitride versus doped silicon nitride.
Using silicon nitride centralizers allows for smaller diameter and higher temperature heaters. A smaller gap is needed between a conductor and a conduit because of the excellent electrical characteristics of the silicon nitride. Silicon nitride centralizers may allow higher operating voltages (for example, up to at least 1500 V, 2000 V, 2500 V, or 15 kV) to be used in heaters due to the electrical characteristics of the silicon nitride.
Operating at higher voltages allows longer length heaters to be utilized (for example, lengths up to at least 500 m, 1000 m, or 1500 m at 2500 V). In some einbodiments, boron nitride is used as a material for centralizers or other electrical insulators. Boron nitride is a better thermal conductor and has better electrical properties than silicon nitride. Boron nitride does not absorb water readily (boron nitride is substantially non-hygroscopic).
Boron nitride is available in at least a hexagonal form and a face centered cubic form. A hexagonal crystalline formation of boron nitride has several desired properties, including, but not limited to, a high thermal conductivity and a low friction coefficient.

Further modifications and alternative embodiments of various aspects of the invention may be apparent to those skilled in the art in view of this description. Accordingly, this description is to be construed as illustrative only and is for the purpose of teaching those skilled in the art the general manner of carrying out the invention. It is to be understood that the forms of the invention shown and described herein are to be taken as the presently preferred embodiments. Elements and materials may be substituted for those illustrated and described herein, parts and processes may be reversed, and certain features of the invention may be utilized independently, all as would be apparent to one skilled in the art after having the benefit of this description of the invention. Changes may be made in the elements described herein without departing from the spirit and scope of the invention as described in the following claims. In addition, it is to be understood that features described herein independently may, in certain embodiments, be combined.

Claims (15)

1. A heating system configurable to heat a subsurface formation, comprising:
an electrical conductor configured to generate an electrically resistive heat output during application of electrical current to the electrical conductor;
an electrical insulator at least partially surrounding the electrical conductor, wherein the electrical insulator comprises a nitride; and a sheath at least partially surrounding the electrical insulator.
2. The system as claimed in claim 1, wherein the nitride is silicon nitride or boron nitride.
3. The system as claimed in claims 1 or 2, wherein the electrical insulator comprises compacted nitride powder.
4. The system as claimed in any of claims 1-3, wherein the electrical insulator comprises one or more substantially annular rings.
5. The system as claimed in any of claims 1-4, wherein the electrical insulator is in direct physical contact with the electrical conductor.
6. The system as claimed in any of claims 1-5, wherein the sheath is in direct physical contact with the electrical insulator.
7. The system as claimed in any of claims 1-6, wherein the electrical conductor is a copper-nickel alloy.
8. The system as claimed in any of claims 1-7, wherein the sheath is a corrosion-resistant material.
9. The system as claimed in any of claims 1-8, wherein the system further comprises two additional electrical conductors, and the electrical conductor and the two additional electrical conductors are configurable in a 3-phase Wye configuration, an electrically floating configuration, or a singly grounded configuration.
10. The system as claimed in any of claims 1-9, wherein the system is configured to heat hydrocarbons in the formation, and to produce heated hydrocarbons from the formation.
11. The system as claimed in any of claims 1-10, wherein the system is configured to transfer heat such that the transferred heat can pyrolyze at least some hydrocarbons in a section of the formation.
12. The system as claimed in any of claims 1-11, wherein the electrical conductor comprises ferromagnetic material, and the system is configured to provide a first heat output when electrical current is applied to the electrical conductor below a selected temperature, and provide a second heat output approximately at and above the selected temperature, the second heat output being less than the first heat output.
13. The system as claimed in any of claims 1-12, wherein the electrical conductor is elongated.
14. An in situ method for heating a formation using the system as claimed in any of claims 1-13, wherein the method comprises:
applying an electrical current to the electrical conductor to provide heat to at least a portion of the formation, wherein the electrical conductor is located in an opening in the formation; and allowing heat to transfer from the electrical conductor to a section of the formation.
15. The method as claimed in claim 14, wherein the method further comprises heating at least some hydrocarbons in the formation such that at least some of the hydrocarbons are pyrolyzed.
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CA2563525A Expired - Fee Related CA2563525C (en) 2004-04-23 2005-04-22 Inhibiting effects of sloughing in wellbores
CA002579496A Abandoned CA2579496A1 (en) 2004-04-23 2005-04-22 Subsurface electrical heaters using nitride insulation
CA2563585A Expired - Fee Related CA2563585C (en) 2004-04-23 2005-04-22 Reducing viscosity of oil for production from a hydrocarbon containing formation
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US20050269091A1 (en) 2005-12-08
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DE602005006115D1 (en) 2008-05-29
WO2005106191A1 (en) 2005-11-10
EP1738058A1 (en) 2007-01-03
CA2563583C (en) 2013-06-18
AU2005238941B2 (en) 2008-11-13
US20050269095A1 (en) 2005-12-08
IL178468A0 (en) 2007-02-11
US20130206748A1 (en) 2013-08-15
CN101107420B (en) 2013-07-24
CN1957158B (en) 2010-12-29
AU2005238944B2 (en) 2008-10-23
CN1946919B (en) 2011-11-16
EP1738052A1 (en) 2007-01-03
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US20050269077A1 (en) 2005-12-08
EP1738053A1 (en) 2007-01-03
NZ550446A (en) 2010-02-26
JP4806398B2 (en) 2011-11-02
US7320364B2 (en) 2008-01-22
US20050269089A1 (en) 2005-12-08
DE602005006116D1 (en) 2008-05-29
EP1738055B1 (en) 2008-11-19
EA200601955A1 (en) 2007-04-27
ATE414840T1 (en) 2008-12-15
US20060289536A1 (en) 2006-12-28
ZA200608260B (en) 2007-12-27
DE602005016096D1 (en) 2009-10-01
EP1738057A1 (en) 2007-01-03
US7510000B2 (en) 2009-03-31
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ZA200608170B (en) 2008-05-28
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US7490665B2 (en) 2009-02-17
US20140231070A1 (en) 2014-08-21
IL178467A (en) 2011-06-30
CA2563589A1 (en) 2005-11-10
WO2005103445A1 (en) 2005-11-03
CA2563525C (en) 2012-07-17
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US7357180B2 (en) 2008-04-15
DE602005011115D1 (en) 2009-01-02
EP1738055A1 (en) 2007-01-03
MXPA06011960A (en) 2006-12-15
US20050269092A1 (en) 2005-12-08
CN1954131B (en) 2012-02-08
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US7481274B2 (en) 2009-01-27
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ATE392535T1 (en) 2008-05-15
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