WO2004063521A2 - Annular fluids and methods of emplacing the same - Google Patents

Annular fluids and methods of emplacing the same Download PDF

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Publication number
WO2004063521A2
WO2004063521A2 PCT/US2004/000456 US2004000456W WO2004063521A2 WO 2004063521 A2 WO2004063521 A2 WO 2004063521A2 US 2004000456 W US2004000456 W US 2004000456W WO 2004063521 A2 WO2004063521 A2 WO 2004063521A2
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WIPO (PCT)
Prior art keywords
fluid
crosslinking
packer
packer fluid
fluids
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PCT/US2004/000456
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English (en)
French (fr)
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WO2004063521A3 (en
Inventor
Andrew G. K. Jones
Bethicia B. Prasek
Robert L. Horton
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M-I L. L. C.
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Priority to BR0406695-2A priority Critical patent/BRPI0406695A/pt
Priority to CA002513066A priority patent/CA2513066C/en
Priority to GB0514414A priority patent/GB2413815B/en
Publication of WO2004063521A2 publication Critical patent/WO2004063521A2/en
Publication of WO2004063521A3 publication Critical patent/WO2004063521A3/en
Priority to NO20053771A priority patent/NO330960B1/no

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    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
    • C09K8/00—Compositions for drilling of boreholes or wells; Compositions for treating boreholes or wells, e.g. for completion or for remedial operations
    • C09K8/50—Compositions for plastering borehole walls, i.e. compositions for temporary consolidation of borehole walls
    • C09K8/504—Compositions based on water or polar solvents
    • C09K8/506—Compositions based on water or polar solvents containing organic compounds
    • C09K8/508—Compositions based on water or polar solvents containing organic compounds macromolecular compounds
    • C09K8/512—Compositions based on water or polar solvents containing organic compounds macromolecular compounds containing cross-linking agents
    • C—CHEMISTRY; METALLURGY
    • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
    • C09K8/00—Compositions for drilling of boreholes or wells; Compositions for treating boreholes or wells, e.g. for completion or for remedial operations
    • C09K8/02—Well-drilling compositions
    • C09K8/04—Aqueous well-drilling compositions
    • C09K8/06—Clay-free compositions
    • C09K8/12—Clay-free compositions containing synthetic organic macromolecular compounds or their precursors
    • E—FIXED CONSTRUCTIONS
    • E21—EARTH DRILLING; MINING
    • E21B—EARTH DRILLING, e.g. DEEP DRILLING; OBTAINING OIL, GAS, WATER, SOLUBLE OR MELTABLE MATERIALS OR A SLURRY OF MINERALS FROM WELLS
    • E21B33/00—Sealing or packing boreholes or wells
    • E21B33/10—Sealing or packing boreholes or wells in the borehole
    • E21B33/12—Packers; Plugs
    • E—FIXED CONSTRUCTIONS
    • E21—EARTH DRILLING; MINING
    • E21B—EARTH DRILLING, e.g. DEEP DRILLING; OBTAINING OIL, GAS, WATER, SOLUBLE OR MELTABLE MATERIALS OR A SLURRY OF MINERALS FROM WELLS
    • E21B33/00—Sealing or packing boreholes or wells
    • E21B33/10—Sealing or packing boreholes or wells in the borehole
    • E21B33/13—Methods or devices for cementing, for plugging holes, crevices, or the like
    • E21B33/138—Plastering the borehole wall; Injecting into the formation
    • E—FIXED CONSTRUCTIONS
    • E21—EARTH DRILLING; MINING
    • E21B—EARTH DRILLING, e.g. DEEP DRILLING; OBTAINING OIL, GAS, WATER, SOLUBLE OR MELTABLE MATERIALS OR A SLURRY OF MINERALS FROM WELLS
    • E21B36/00—Heating, cooling, insulating arrangements for boreholes or wells, e.g. for use in permafrost zones

Definitions

  • the invention relates generally to viscosifiable, low thermal conductivity annular fluids and methods of viscosifying, emplacing, and removing the fluids.
  • Annular fluids or packer fluids are liquids which are pumped into an annular opening between a casing and a wellbore wall or between adjacent, concentric strings of pipe extending into a wellbore. These fluids are especially necessary in oil or gas well construction operations conducted in low temperature venues of the world, for example, those areas having permafrost.
  • Permafrost is a thick layer of frozen surface ground which may be several hundred feet thick and presents a great obstacle to the removal of relatively warm fluids through a well pipe.
  • warm fluid in the well pipe causes thawing of the permafrost in the vicinity of the well resulting in subsidence which can impose compressive and/or tension loads high enough to rupture or collapse the well casing and hence allow the escape of well fluids.
  • the warm gas or oil coming to the surface in the well pipe becomes cooled by giving up its heat to the permafrost.
  • gas hydrate crystals may form, which can freeze together and block the well pipe.
  • annular heat loss is due to convection and to conduction.
  • Heavy oil production is another operation which often can benefit from the use of an insulating annular fluid.
  • a high-pressure steam or hot water is injected into the well and the oil reservoir to heat the fluids in the reservoir, causing a thermal expansion of the crude oil, an increase in reservoir pressure and a decrease of the oil's viscosity.
  • damage to the well casing may occur when heat is transferred through the annulus between the well tubing and the casing.
  • the resulting thermal expansion of the casing can break the bond between the casing and the surrounding cement, causing leakage.
  • an insulating medium such as a packer fluid may be used to insulate or to help insulate the well tubing.
  • the packer fluid also reduces heat loss and saves on the energy requirements in steam flooding.
  • subsea fields especially, subsea fields in deep water, 1,500 to more than 6,000 feet deep — require specially designed systems which typically require a packer fluid.
  • a subsea oil reservoir temperature may be between about 120°F and 250°F, while the temperature of the water through which the oil must be conveyed is often as low as 32° F to 50° F.
  • Conveying the high temperature oil through such a low temperature environment can result in oil temperature reduction and consequently the separation of the oils into various hydrocarbon fractions and the deposition of paraffins, waxes, asphaltenes, and gas hydrates.
  • the agglomeration of these oil constituents can cause blocking or restriction of the wellbore, resulting in significant reduction or even catastrophic failure of the production operation.
  • U.S. Pat. No. 3,613,792 describes an early method of insulating wellbores.
  • simple fluids and solids are used as the insulating medium.
  • U.S. Pat. No. 4,258,791 improves on these insulating materials by disclosing an oleaginous liquid such as topped crude oils, gas oils, kerosene, diesel fluids, heavy alkylates, fractions of heavy alkylates and the like in combination with an aqueous phase, lime, and a polymeric material.
  • 4,528,104 teaches a packer fluid comprised of an oleaginous liquid such as diesel oil, kerosene, fuel oil, lubricating oil fractions, heavy naphtha and the like in combination with an organophillic clay gellant and a clay dispersant such as a polar organic compound and a polyfunctional amino silane.
  • U.S. Pat. No. 4,877,542 teaches a thermal insulator fluid consisting of a heavy mineral oil as the major liquid portion, a light oil as a minor liquid portion, a smectite-type clay, calcium oxide and hydrated amorphous sodium silicate.
  • U.S. Pat. No. 5,290,768 teaches a thixotropic composition containing ethylene glycol and welan gum. The above-discussed patents are herein incorporated by reference.
  • Dewprashad '694 (hereinafter referred to as "Dewprashad '694").
  • Holtmyer '620, Weaver '057, and Dewprashad '694 discuss the viscosification of brines using crosslinked hydroxyethylcellulose derivatives. These patents are hereby incorporated by reference.
  • the present invention relates to a packer fluid that includes a water-miscible solvent, a viscosifying additive, a crosslinking agent having the facility to crosslink the viscosifying additive, a crosslinking inhibitor adapted to inhibit crosslinking between the viscosifying additive and the crosslinking agent, and an initiating agent having the facility to overcome an action of the crosslinking inhibitor and to initiate crosslinking between the viscosifying additive and the crosslinking agent.
  • the packer fluid has a thermal conductivity of no more than about 0.25 btu/(hr ft- °F), and a potential to substantially increase its viscosity upon sitting for a selected period of time.
  • the present invention relates to a method for preparing a packer fluid that includes mixing a water-miscible solvent and a viscosifying additive to produce a first fluid, acidifying the first fluid with an acid to produce a second fluid, adding a crosslinking agent to the second fluid to produce a third fluid, and adding an initiating agent to the third fluid to permit crosslinking between the viscosifying additive and the crosslinking-agent.
  • the present invention relates to a method for emplacing a packer fluid into an annulus that includes preparing a packer fluid, pumping the packer fluid into the annulus before the selected period of time, and allowing the packer fluid to sit in the annulus such that the viscosity of the packer fluid is substantially increased.
  • the present invention relates to insulating packer fluids, and methods of emplacing and subsequently removing such fluids.
  • Packer fluids according to the present invention have very low thermal conductivities, while simultaneously meeting other constraints (e.g., regulatory or environmental constraints) imposed upon the packer fluids. These fluids are facile to pump, yet are capable of becoming very viscous after they are resident in situ within the annular space or one of the annular spaces in an oil or gas well.
  • Prior art packer fluids often are oil-based (hydrocarbon-based) because oil-based fluids typically have very low thermal conductivities. For example, thermal conductivities as low as 0.07 btu/(hr- ft- °F) can be obtained with gelled diesel or other hydrocarbon-based insulating annular fluid. As noted above, these fluids typically have adverse environmental effects and are not desirable.
  • water-based and water-miscible fluids are, in many cases, preferred in spite-of the fact that- water-based fluids typically have much- higher- -thermal conductivities because water has a thermal conductivity of 0.351 btu/(hr ft- °F).
  • aqueous solutions While most aqueous solutions have thermal conductivities as predicted by this equation, some exceptions do exist. For example, concentrated sulfuric acid (90%) has a thermal conductivity that is 8.8% below the predicted value, and a 30% dilute sulfuric acid has a thermal conductivity that is 16.5% below the predicted value. Similarly, thermal conductivities of concentrated sucrose solutions fall substantially below the predicted values (up to about 29% below the predicted values). The same phenomenon is also observed with non- aqueous water-miscible solutions such as ethylene glycol, propylene glycol, and solutions of various salts such as calcium bromide in ethylene glycol or propylene glycol. These solutions can have thermal conductivities that are as much as 60% lower than the predicted values.
  • Embodiments of the present invention relate to low thermal conductivity annular fluids based on water-miscible fluids (e.g., various glycols), which have been formulated to have the desired rheological properties.
  • these annular fluids are formulated to have certain viscosities for facile pumping of these fluids into an annular space. However, they will develop substantially increased viscosities in situ after they have been emplaced in the annular space. In other words, these fluids have delayed viscosifying properties.
  • Narious formulations of fluids within the scope of the present invention are provided below as examples. However, the present invention is not limited to the described embodiments, but is bounded by the claims that follow.
  • a fluid having a density of 9.86 ppg and a ⁇ of about 0.14 btu/(hr- ft- °F) was formulated from the following components:
  • ECF 680 is a slurry of a doubly derivatized hydroxyethyl cellulose
  • DDHEC inert, water-miscible carrier fluid.
  • ECF 680 is available commercially from M-I L.L.C. (Houston, TX).
  • DDHEC may be synthesized by grafting monomers of vinyl phosphonic acid (NPA) onto cellulose polymers according to methods disclosed in U.S. Patent No. 5,304,620 (Holtmyer '620).
  • the components were added in the order listed in the table.
  • the first two components ethylene glycol and ECF 680, were mixed and stirred together for about 1 hour to thoroughly disperse the polymer in the ethylene glycol.
  • 2.38 grams of concentrated ( ⁇ 38.5 wt%) hydrochloric acid were added and stirring was continued for about 30 minutes.
  • the mixture was set aside and its viscosity was observed over the course of 4 hours. At first, the viscosity was approximately that of ethylene glycol, but after about 2 hours, the viscosity increased substantially, to about 300 cP when measured at 200 rpm on a Fann 35A viscometer.
  • magnesium oxide neutralizes the acid and raises the pH to the 8 - 9 range, whereupon divalent or multi-valent cations (e.g., Ca 2+ ) already present in the mixture crosslink DDHEC.
  • divalent or multi-valent cations e.g., Ca 2+
  • other polymers similar to DDHEC could be used (e.g., similarly modified cellulose, guar, or hydroxypropyl guar), and the multi-valent or divalent cations may be added separately.
  • the crosslinking does not occur immediately, but instead occurs over the ' course of several hours, leading to doubling of the apparentrviscosity of the- mixture during these several hours and gradually increasing to about 50 percent of its ultimate value upon sitting overnight at room temperature. Only after sitting at room temperature for several days did the mixture achieve its ultimate viscosity, that of a semi-rigid gel.
  • the delayed viscosifying property of this embodiment permits facile emplacement of this fluid into an annular space, while the ultimate viscosity of this fluid is desirable for arresting or substantially reducing heat loss due to convection.
  • Example 1 Because the embodiment of Example 1 has desirable properties for use as an annular fluid, the process of initiating polymer crosslinking by addition of MgO is investigated in more detail.
  • a fluid having a density of 9.86 ppg and a ⁇ of about 0.14 btu/(hr- ft- °F) was formulated similarly to Example 1, except that the magnesium oxide was not added as a slurry in ethylene glycol but as a dry powder. The magnesium oxide was found to be able to disperse thoroughly throughout the mixture without causing any locally high pH pocket that might lead to premature crosslinking.
  • the crosslinking occurred over the course of several hours, leading to an increase in the viscosity.
  • a fluid having a density of 9.86 ppg and a ⁇ of about 0.14 btu/(hr- ft- °F) was formulated similarly to Example 1, except that the magnesium oxide was a very fine powder in a highly reactive form, i.e., having small particle size, high surface area, and ready accessibility for reaction.
  • a fine powder MgO is available commercially from M-I L.L.C under the trade name of Di-BalanceTM.
  • the fine powder MgO was added as a slurry in ethylene glycol.
  • the magnesium oxide was found to be able to disperse thoroughly throughout the mixture without causing any locally high pH pocket that might lead to premature crosslinking. As in Example 1, the crosslinking occurred over the course of several hours, leading to an increase in the viscosity.
  • the divalent cation (Ca 2+ ) is prevented from crosslinking DDHEC by the addition of acid (HCl). Subsequent addition of MgO counters the effect of HCl and allows the crosslinking to take place. Surprisingly, the order of the addition of the divalent cation and the acid has a dramatic effect on the ability of the resultant fluid to viscosify, as evidenced by the following example.
  • a fluid having a density of 9.86 ppg and a ⁇ of about 0.14 btu/(hr- ft- °F) was formulated from the same components as in Example 1, but in the following order:
  • the components were added in the order listed in the table.
  • the first two components ethylene glycol and ECF 680
  • the first two components were mixed and stirred together for about 1 hour to thoroughly disperse the polymer into the ethylene glycol.
  • the dry calcium chloride was added, liberating heat as the solid dissolved in the mixture.
  • the calcium chloride was added in a controlled manner to prevent the temperature from rising high enough to thermally degrade the DDHEC.
  • step 7 A detectable increase in heat resulted upon the addition of the calcium bromide to the ethylene glycol.
  • the mixture in the second jar was stirred while the mixture first heated, then cooled (step 7).
  • step 7 When the product of step 7 had cooled to room temperature, 8.0 grams of the solution was removed.
  • step 8 To the removed 8.0 grams of solution, the following was added (step 8):
  • step 8 While the 2 grams of MgO was being mixed with the 8.0 grams of solution (step 8), the rest of the product from step 7 was rapidly mixed into the thick slurry produced in step 5 (step 9).
  • step 10 When these two fluids were thoroughly mixed, at least 95% of the slurry from step 8 was mixed into the product of step 9 (step 10).
  • step 10 The product of step 10 was then set aside so that the crosslinking reaction could proceed. Crosslinking did not occur immediately, but over the course of several hours, leading to the doubling of the apparent viscosity of the mixture during these several hours. The apparent viscosity of the mixture gradually increased to about 50 percent of its ultimate value upon sitting overnight at room temperature. Only after sitting at room temperature for several days did the mixture achieve its ultimate viscosity, that of a semi-rigid gel.
  • step 5 The reagents were added in the above order. The mixture was then stirred for about 30 minutes. To this mixture, the following was added (step 5):
  • step 7 The mixture in the second jar was stirred while the mixture first heated, then cooled (step 7). When the product of step 7 had cooled to room temperature, 8.0 grams of the solution was removed. To the removed 8.0 grams of solution, the following was added (step 8):
  • step 7 8. 2.0 gms. of MgO. (0.4% by wt.) [0043] While the magnesium oxide was becoming wetted with the 8.0 grams of solution, the remaining product of step 7 was mixed into the thick slurry produced in step 5 (step 9). When these two fluids were thoroughly mixed, at least 95% of the slurry from step 8 was mixed into the rapidly mixed product of step 9 (step 10).
  • step 10 The product of step 10 was then set aside so that the crosslinking reaction could proceed. Crosslinking did not occur immediately, but over the course of several hours, leading to the doubling of the apparent viscosity of the mixture during these several hours. The apparently viscosity of the mixture gradually increased to about 50 percent of its ultimate value upon sitting overnight at room temperature. Only after sitting at room temperature for several days did the mixture achieve its ultimate viscosity, that of a semi-rigid gel. This example shows that relative proportions of calcium bromide used have no significant effect on the ultimate viscosity of the fluid.
  • ultimate viscosities of the annular fluids result from crosslinking DDHEC by the divalent ions.
  • the amounts of DDHEC in these fluids should have significant effects on the final viscosities of the fluids.
  • the following two examples illustrate the effects of the DDHEC concentrations on the viscosities of the resultant fluids.
  • a fluid having a similar density and thermal conductivity as those in examples 5 and 6, i.e., density of 10.8 ppg and a ⁇ of about 0.20 b ⁇ tu/(hr " ft r" °F)7 was formulated as follows:
  • step 7 A detectable increase in heat resulted upon the addition of the calcium bromide to the ethylene glycol.
  • the mixture in the second jar was stirred while the mixture first heated, then cooled (step 7).
  • step 7 When the product of step 7 had cooled to room temperature, 8.0 grams of the solution was removed.
  • step 8 To the removed 8.0 grams of solution, the following was added (step 8):
  • step 9 While the magnesium oxide was becoming wetted with the 8.0 grams of solution, the remaining product of step 7 was mixed into the thick slurry produced in step 5 (step 9). When these two fluids were thoroughly mixed, at least 95% of the slurry from step 8 was mixed into the product of step 9 (step 10). The product of step 10 was then set aside so that the crosslinking reaction could proceed.
  • step 5 The reagents were added in the above order. The mixture was then stirred for about 30 minutes. To this mixture, the following was added (step 5):
  • step 7 A detectable increase in heat resulted upon the addition of the calcium bromide to the ethylene glycol.
  • the mixture in the second jar was stirred while the mixture first heated, then cooled (step 7).
  • step 7 When the product of step 7 had cooled to ⁇ room temperature, 8.0 grams of the solution was removed.
  • step 8 To th ⁇ -T removed 8.0 grams of solution, the following was added (step 8):
  • step 7 While the magnesium oxide was becoming wetted with the 8.0 grams of solution, the remaining product of step 7 was mixed into the thick slurry produced in step 5. [0055] When these two fluids were thoroughly mixed, at least 95% of the slurry from step 8 was mixed into the product of step 9 (step 10). The product of step 10 was then set aside so that the crosslinking reaction could proceed.
  • a fluid having a density of 10.8 ppg and a ⁇ of about 0.16 btu/(hr- ft- °F) was formulated from the following components:
  • This embodiment has a similar composition as that of Example 1, except that .so iumjjr mide s used instead of calcium bromide.
  • the components were added in the order listed above. The first two components were mixed and stirred together for about 1 hour to thoroughly disperse the polymer into the ethylene glycol. Then 2.38 grams of concentrated ( ⁇ 38.5 wt%) hydrochloric acid were added, and stirring was continued for about 30 minutes. The mixture was set aside and its viscosity was observed over the ensuing 4 hours. At first the viscosity was approximately that of ethylene glycol, but after about 2 hours the viscosity increased substantially to about 300 cP when measured at 200 rpm on a Fann 35 A viscometer.
  • composition comprises identical components in the same amounts as those in Example 9. The components were added in the order listed above.
  • the first two components were mixed and stirred together for about 1 hour to thoroughly disperse the polymer into the ethylene glycol. Then dry sodium bromide was added (no significant liberation of heat was observed). Next, 2.38 grams of concentrated ( ⁇ 38.5 wt%) hydrochloric acid were added, and stirring was continued for about 30 minutes.
  • Example 4 shows that the order of addition of the components is important, and, for best results, the salt (e.g., sodium bromide or calcium bromide) addition should be delayed until after the acid has been added.
  • the salt and sodium bromide did not completely inhibit the hydration, yielding, and subsequent crosslinking of the polymer.
  • a fluid having a density of 9.86 ppg and a ⁇ of about 0.14 btu/(hr- ft- °F) was formulated from the following components:
  • Example 1 This composition is identical to that of Example 1.
  • the components were also added in the same order as in Example 1, i.e., as listed above.
  • the components were mixed as described in Example 1.
  • the fluid was not allowed to sit overnight at room temperature to crosslink. Instead, the mixture was placed in a 180°F oven for one hour, taken out and cooled to room temperature, and its viscosity was assessed. At this point, the viscosity had visibly increased, indicating the onset of crosslinking. However, at this point, the fluid was still readily pourable from one container to another.
  • embodiments of the invention can provide packer fluids or annular fluids which have low thermal conductivities, can be pumped easily, and will become substantially viscosified upon emplacement, whereupon they will become substantially incapable of conducting heat through convection, and consequently will have low total heat- loss.
  • Embodiments of the invention use water miscible glycols to formulate fluids with low thermal conductivities.
  • ethylene glycols e.g., diethylene glycol, triethylene glycol, tetraethylene glycol, propylene glycol, dipropylene glycol, tripropylene glycol, tetrapropylene glycol, and the like
  • alcohol-glycol ethers e.g., ethylene glycol monobutyl ether, methyl diethylene glycol, ethyl triethylene glycol, propyl tetraethylene glycol, ethyl propylene glycol, methyl dipropylene glycol, propyl tripropylene glycol, and the like
  • alcohols may be used without departing from the scope of the invention.
  • water miscible solvents may be used.
  • concentrations of the water miscible solvents may depend on the desired thermal conductivities and the type of water miscible solvents.
  • ethylene glycol is used at a concentration of 54% - 78% by weight in the final fluids. These fluids have thermal conductivities of 0.2 btu/(hr- ft- °F) or less. In examples 5 - 8, up to about 10% by weight of water is included, while ethylene glycol is present at about 54% - 61% by weight. These fluids, nevertheless, have relatively low thermal conductivities (about 0.2 btu/(hr- ft- °F)).
  • doubly derivatized hydroxyethyl -cellulose _ (DDHEC) is used to thicken the fluids.
  • the derivatization is by reacting HEC with vinyl phosphonic acid.
  • One of ordinary skill in the art would appreciate other similar polymers may be used, such as derivatized hydroxypropyl cellulose or derivatized cellulose. These polymers thicken upon crosslinking with divalent or polyvalent ions.
  • Other polymers that thicken by different mechanisms may also be used.
  • guars or celluloses, with or without derivatization may be crosslinked with boron, titanium, or zirconium.
  • DDHEC may be conveniently used in a slurry form, such as that sold under the trade name of ECF 680TM by M-I, L.L.C. (Houston, TX).
  • ECF 680TM 1.9% to about 3.7% by weight of ECF 680TM.
  • the ultimate viscosities of the fluids depend upon the amounts of DDHEC used. The above examples clearly show that high viscosities (e.g., that of a semi-solid) can be achieved at a DDHEC concentration of about 3.7% by weight of ECF 680TM. Even at lower concentrations of DDHEC, appreciable thickening of the fluids was achieved.
  • the divalent or polyvalent ions that crosslink DDHEC or the like may come from salts (e.g., CaBr 2 ) that are present in the fluids before a Lewis base or a Bronsted-Lowry base (e.g., MgO) is added to initiate the crosslinking, or from the Lewis base or a Bronsted-Lowry base (e.g., MgO) itself. While MgO is used in the above examples, one of ordinary skill in the art would appreciate that other Lewis base or a Bronsted-Lowry base, such as BaO, CaO, or the like, may be used without departing from the scope of the invention.
  • salts e.g., CaBr 2
  • MgO Bronsted-Lowry base
  • alkaline metal or alkaline-earth metal hydroxides e.g., NaOH, KOH, etc.
  • bases may also be used to raise the pH and to initiate the crosslinking if the fluids already include divalent or polyvalent ions.
  • an annular fluid using, for example, the DDHEC polymer as the viscosifier additive, may be prepared as follows:
  • DDHEC polymer slurry pails are stirred to thoroughly re-disperse any settled polymer into the slurry.
  • the slurry preferably is stirred until it is smooth and its color is uniform before adding to a completion fluid or other fluids.
  • DDHEC polymer slurry is added into the blender over the top.
  • a typical dosage is one ⁇ 5.4 gallon pail ( ⁇ 50 lb) per 3 bbl fluid.
  • the final viscosity is typically about 160 to 240 cP, depending on fluid and temperature. In some cases, hydration should be complete within 20 to 90 minutes, especially with fluids having substantial amounts of free water; for other fluids, especially those having a higher glycol content, hydration may take longer.
  • the magnesium oxide is prepared for addition to the mixture.
  • the recommended magnesium oxide loading is about 1 lb/bbl of gelled fluid.
  • 1.25 lb/bbl of magnesium oxide is recommended.
  • the required amount of the magnesium oxide is mixed into 11.6 ppg CaCl 2 brine at 10 lbs/3 gal.
  • the magnesium oxide/fluid slurry is preferably used within 2 hours after mixing. Otherwise, it will harden if stored for later use.
  • the gel is circulated through " the ⁇ eductor port on the top of the blender. While circulating, the- magnesium oxide slurry is slowly added into the blender through the eductor port. The jetting action of the circulating gel helps to evenly disperse the magnesium oxide slurry. If sufficient crosslinking has not begun to occur within 15 minutes, slurry an additional ⁇ lb ./per bbl. of the magnesium oxide for addition to the mixture through the eductor port. [0084] At this time, when some viscosity has developed, but well before a substantial fraction of the fluid has had an opportunity to crosslink, the mixture is ready for emplacement.
  • the crosslinking process should not be initiated (by the addition of the magnesium oxide) until timing is appropriate for prompt placement of the mixture.
  • Crosslink time is influenced by several factors including: a. Fluid type
  • Calcium-based brines crosslink more quickly, decreasing crosslink time.
  • any excess fluid in connecting piping, valves, manifolds, etc. should be displaced before the fluid has had time enough to thoroughly crosslink.
  • the fluid will remain essentially free of convective currents that are responsible for convective heat-loss through the annulus.
  • the only remaining heat-loss avenues are radiative heat-loss, which is ordinarily negligible in magnitude, and conductive heat-loss, which is minimized through the selection of a low-thermal-conductivity base fluid for the mixture.
  • Hydrochloric acid can be spotted upon or atop the crosslinked fluid instead, but this method requires a much longer break time. Several days may -be required to fully- break the mixture if diffusion is relied upon to.disfribute the.. hydrochloric acid to break through the crosslinked fluid.
  • the present invention advantageously discloses novel compositions for use as insulating packer fluids and methods for emplacing the same.
  • Insulating packer fluids are designed to reduce heat loss due to conduction and convection when emplaced in the annular space in an oil or gas well or to assist in reducing heat loss due to conduction and convection when emplaced in one of the annular spaces in an oil or gas well.
  • conventional insulating packer fluids reduce conductive heat loss primarily by being formulated from base fluids that have inherently low coefficients of thermal conductivity, and they reduce convective heat loss primarily by being formulated with viscosifying additives that are so viscous from the very beginning, once the fluid is fully formulated, and throughout the useful life of the fluid, that convection currents are arrested or substantially diminished.
  • Embodiments of the present invention advantageously provide insulating packer fluids that are very low in thermal conductivity while simultaneously meeting all of the other constraints imposed upon the packer fluid.
  • Preferred embodiments of the present invention are based on compositions that are 25 to 100% ethylene glycol (or other suitable chemicals having the requisite properties described above).
  • embodiments of the present invention are easier to pump yet become more viscous than conventional fluids when the insulating packer fluids are resident in situ within the annular space or one of the annular spaces in an oil or gas well. This is accomplished by incorporating a crosslinkable viscosifying additive into the novel compositions taught herein.
  • Other compositions in accordance with the present invention comprise blends of conventional insulating packer fluids with those that include crosslinkable viscosifying additives.
  • Typical brine-based well fluid viscosifying additives include natural and synthetic polymers and oligomers.
  • the viscosifying additives suitable for embodiments of the present invention include poly(ethylene glycol) (PEG), poly(diallyl amine), poly(acrylamide), poly(aminomethylpropyl-sulfonate [AMPS]), poly(acrylonitrile), poly(vinyl acetate), poly(vinyl --alc.o-hol),-.-.pQly(yinyl._amjne).,-_-p( ⁇ y(yiny _ sulfonate), . - .
  • R 1 is hydrogen, methyl or ethyl
  • R 2 is the group -COOR 4 , the sulfonyl group, the phosphonyl group, the phosphonyl group esterified by (C ⁇ -C 4 )-alkanol or a group of the formula
  • R 3 is hydrogen, methyl, ethyl or the carboxyl group
  • R 4 is hydrogen, arnino or hydroxy-(CrC 4 )-alkyl
  • R 5 is the sulfonyl gr ⁇ up, tne " ph spfaohyT group or the carboxyl group, or grafting (co)polymerization of one or more hydrophilic monomers of the formula I onto a grafting base, using a free radical initiator which forms three or more free radical sites per molecule, or monomers of the formula II:
  • X 2 O 3 PCHYCZ 2 PO 2 XH where X is H, alkali metal or ammonia, Y and Z are each H, PO X 2 , SO 3 X or CO 2 X (e.g., vinyl phosphonic acid or vinylidene diphosphonic acid) or groups which react with hypophosphorous acid in the presence of free radicals providing compounds X 2 O 3 PCHYCZ 2 PO 2 XH which react with monomers such as vinyl sulfonate, vinylphosphonate, vinylidene diphosphonate and acrylic acid.
  • monomers such as vinyl sulfonate, vinylphosphonate, vinylidene diphosphonate and acrylic acid.
  • the viscosifying additives suitable for embodiments of the present invention also include "natural" polymers onto which have been grafted one or more co-, ter-, and quater-monomers of the following: ethylene, butadiene, isoprene, styrene, divinylbenzene, divinyl amine, l,4-pentadiene-3-one (divinyl ketone), l,6-heptadiene-4-one (diallyl ketone), diallyl amine, ethylene glycol, acrylamide, AMPS, acrylonitrile, vinyl acetate, vinyl alcohol, vinyl amine, vinyl sulfonate, styryl sulfonate, acrylate, methyl acrylate, methacrylate, methyl methacrylate, vinylpyrrolidone, vinyl lactams, vinyl phosphonate, bis- ( ⁇ -chloroethyl vinyl phosphonate) ⁇ also known as bis(2-chlor
  • R 1 is hydrogen, methyl or ethyl
  • R 2 is the group -COOR 4 , the sulfonyl group, the phosphonyl group, the phosphonyl group esterified by (C ⁇ -C 4 )-alkanol or a group of the formula
  • R is hydrogen, methyl, ethyl or the carboxyl group
  • R is hydrogen, amino or hydroxy-(C ⁇ -C 4 )-alkyl
  • R 5 is the sulfonyl group, the phosphonyl group or the carboxyl group, or grafting (co)polymerization of one or more hydrophilic monomers of the formula I onto a grafting base, using a free radical initiator which forms three or more free radical sites per molecule, or monomers of the formula II:
  • X 2 O 3 PCHYCZ 2 PO 2 XH where X is H, alkali metal or ammonia, Y and Z are each H, PO 3 X 2 , SO 3 X or CO 2 X (e.g., vinyl phosphonic acid or vinylidene diphosphonic acid) or groups which react with hypophosphorous acid in the presence of free radicals providing compounds X O 3 PCHYCZ 2 PO 2 XH which react with monomers such as vinyl sulfonate, vinylphosphonate, vinylidene diphosphonate and acrylic acid.
  • monomers such as vinyl sulfonate, vinylphosphonate, vinylidene diphosphonate and acrylic acid.
  • Suitable crosslinking agents in accordance with the present invention include (1) "crosslinking agents active upon vicinal diol groups", i.e., a borate, titanate, or zirconate crosslinkants as taught in U.S. Patent No. 5,062,969, (2) divalent, trivalent, or tetravalent cations such as, for example, Fe 2+ , Cd 2+ , Co 2+ , Ca 2+ , Cu 2+ , UO 2 2+ , PbO 2+ , Al 3+ , Fe 3+ , Cr 3+ , Ce 3+ , Ti 4+ , Zr 4+ , Sn 4+ , and the like, (3) complexes of or other moieties containing the crosslinkants listed above in the first two categories, such as, j for example, the teframmine complex of the Cu 2+ cation, the carbonate anion complexes of the UO 2 2+ cation, UO 2 (CO 3 ) 2 2" and UO (
  • brine solutions such as ZnCl 2 , CaCl 2 , CaBr 2 , ZnBr 2 , NaHCO 2 , KHCO 2 , CsHCO 2 , NaCl, KC1, NH 4 C1, MgCl 2 , seawater, NaBr, KBr, CsBr, and combinations thereof may be used in connection with the present invention.
  • embodiments of the present invention disclose making an annular fluid as thick as possible prior to crosslinking so that the fluid is readily pumpable. Further, embodiments of the present invention disclose subsequently adding a crosslinking activator during the process of pumping the fluid so that the fluid will not gain viscosity due to crosslinking while the fluid is being pumped, but will gain viscosity to a very substantial extent later when the fluid is resident in situ within the annular space .or. one of the annular spaces in an oil or gas well. Therefore,- embodiments of the present invention advantageously provide an annular fluid that controls annular heat loss due to convection and to conduction.
  • promoter it is expressly within the scope of the present invention to use fluids having a thermal conductivity of no more than about 0.25 btu/(hr- ft- °F), which include a water-miscible solvent and a viscosifying additive, wherein the packer fluid has an inherent capability to substantially increase its viscosity upon sitting for a selected period of time, hi certain embodiments, therefore, low thermal conductivity fluids may be used that viscosity simply after being emplaced in a well or through other triggering mechanisms known to those in the art.
PCT/US2004/000456 2003-01-09 2004-01-09 Annular fluids and methods of emplacing the same WO2004063521A2 (en)

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BR0406695-2A BRPI0406695A (pt) 2003-01-09 2004-01-09 Fluido de obturador, processo para a preparação de um fluido de obturador e processo para sua instalação em um anel tubular
CA002513066A CA2513066C (en) 2003-01-09 2004-01-09 Annular fluids and methods of emplacing the same
GB0514414A GB2413815B (en) 2003-01-09 2004-01-09 Annular fluids and methods of emplacing the same
NO20053771A NO330960B1 (no) 2003-01-09 2005-08-08 Viskositetsokende pakningsfluid med termisk konduktivitet

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US7829509B2 (en) 2010-11-09
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BRPI0406695A (pt) 2005-12-20
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GB2413815A (en) 2005-11-09
NO20053771D0 (no) 2005-08-08

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