WO2020005443A1 - Methods of controlling fines migration in a well - Google Patents
Methods of controlling fines migration in a well Download PDFInfo
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- WO2020005443A1 WO2020005443A1 PCT/US2019/034338 US2019034338W WO2020005443A1 WO 2020005443 A1 WO2020005443 A1 WO 2020005443A1 US 2019034338 W US2019034338 W US 2019034338W WO 2020005443 A1 WO2020005443 A1 WO 2020005443A1
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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
- C09K8/56—Compositions for consolidating loose sand or the like around wells without excessively decreasing the permeability thereof
- C09K8/57—Compositions based on water or polar solvents
- C09K8/575—Compositions based on water or polar solvents containing organic compounds
- C09K8/5751—Macromolecular compounds
-
- 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
- C09K8/516—Compositions for plastering borehole walls, i.e. compositions for temporary consolidation of borehole walls characterised by their form or by the form of their components, e.g. encapsulated material
-
- 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
- C09K8/60—Compositions for stimulating production by acting on the underground formation
- C09K8/62—Compositions for forming crevices or fractures
- C09K8/66—Compositions based on water or polar solvents
- C09K8/68—Compositions based on water or polar solvents containing organic compounds
-
- 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
- C09K8/60—Compositions for stimulating production by acting on the underground formation
- C09K8/62—Compositions for forming crevices or fractures
- C09K8/70—Compositions for forming crevices or fractures characterised by their form or by the form of their components, e.g. foams
-
- 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
- C09K8/60—Compositions for stimulating production by acting on the underground formation
- C09K8/62—Compositions for forming crevices or fractures
- C09K8/72—Eroding chemicals, e.g. acids
- C09K8/74—Eroding chemicals, e.g. acids combined with additives added for specific purposes
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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
- C09K8/60—Compositions for stimulating production by acting on the underground formation
- C09K8/80—Compositions for reinforcing fractures, e.g. compositions of proppants used to keep the fractures open
-
- 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
- C09K8/60—Compositions for stimulating production by acting on the underground formation
- C09K8/80—Compositions for reinforcing fractures, e.g. compositions of proppants used to keep the fractures open
- C09K8/805—Coated proppants
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- E—FIXED CONSTRUCTIONS
- E21—EARTH OR ROCK DRILLING; MINING
- E21B—EARTH OR ROCK DRILLING; OBTAINING OIL, GAS, WATER, SOLUBLE OR MELTABLE MATERIALS OR A SLURRY OF MINERALS FROM WELLS
- E21B43/00—Methods or apparatus for obtaining oil, gas, water, soluble or meltable materials or a slurry of minerals from wells
- E21B43/02—Subsoil filtering
- E21B43/04—Gravelling of wells
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- E—FIXED CONSTRUCTIONS
- E21—EARTH OR ROCK DRILLING; MINING
- E21B—EARTH OR ROCK DRILLING; OBTAINING OIL, GAS, WATER, SOLUBLE OR MELTABLE MATERIALS OR A SLURRY OF MINERALS FROM WELLS
- E21B43/00—Methods or apparatus for obtaining oil, gas, water, soluble or meltable materials or a slurry of minerals from wells
- E21B43/16—Enhanced recovery methods for obtaining hydrocarbons
- E21B43/20—Displacing by water
-
- E—FIXED CONSTRUCTIONS
- E21—EARTH OR ROCK DRILLING; MINING
- E21B—EARTH OR ROCK DRILLING; OBTAINING OIL, GAS, WATER, SOLUBLE OR MELTABLE MATERIALS OR A SLURRY OF MINERALS FROM WELLS
- E21B43/00—Methods or apparatus for obtaining oil, gas, water, soluble or meltable materials or a slurry of minerals from wells
- E21B43/25—Methods for stimulating production
- E21B43/26—Methods for stimulating production by forming crevices or fractures
-
- E—FIXED CONSTRUCTIONS
- E21—EARTH OR ROCK DRILLING; MINING
- E21B—EARTH OR ROCK DRILLING; OBTAINING OIL, GAS, WATER, SOLUBLE OR MELTABLE MATERIALS OR A SLURRY OF MINERALS FROM WELLS
- E21B43/00—Methods or apparatus for obtaining oil, gas, water, soluble or meltable materials or a slurry of minerals from wells
- E21B43/25—Methods for stimulating production
- E21B43/26—Methods for stimulating production by forming crevices or fractures
- E21B43/267—Methods for stimulating production by forming crevices or fractures reinforcing fractures by propping
Definitions
- the disclosure is directed to methods of treating subterranean formations. More specifically, the disclosure relates to methods of controlling fines migration in a well.
- Fines may result from an unconsolidated or inherently unstable formation, or from the use of an incompatible treatment fluid that liberates fine particles.
- Other sources of fines include particulates added to the wellbore such as fines present in a proppant or produced from partially crushed proppant.
- formation fines may migrate toward the near wellbore area due to drag or other forces.
- the migrated fines can plug, erode or cause significant wear of downhole equipment and surface facilities.
- the fines can also plug or clog flow channels in the formation, thereby significantly reducing well productivity.
- a method of treating a subterranean formation penetrated by a wellbore comprises: introducing into the subterranean formation a treatment fluid comprising coated polymeric particles having a polymeric core and a curable thermoset coating disposed on the polymeric core, the polymeric core comprising a rubber, an epoxy, a phenolic resin, a thermoplastic polymer or a combination comprising at least one of the foregoing, the rubber comprising a nitrile rubber (NBR), a hydrogenated nitrile rubber (HNBR), a styrene- butadiene rubber (SBR), an ethylene propylene diene monomer rubber (EPDM), a natural rubber, a silicone rubber, a polybutadiene, polyisoprene, butyl rubber, or a combination comprising at least one of the foregoing, and the thermoplastic polymer comprising polyetheretherketone (PEEK), a polyimide, a polysulfone, a polyester or polycarbon
- Coated polymeric particles comprises: a recycled polymeric core in a particulate form, and a curable coating disposed on the polymeric core, wherein recycled polymeric core has a size of about 3.5 to 40 mesh and comprises nitrile rubber (NBR), hydrogenated nitrile rubber (HNBR), styrene-butadiene rubber (SBR), ethylene propylene diene monomer rubber (EPDM), natural rubber, silicone rubber, polybutadiene, polyisoprene, butyl rubber, rubber blend, polyetheretherketone (PEEK), polyamide, polyimide, polysulfone, polyester, polycarbonate, or a combination comprising at least one of the foregoing.
- NBR nitrile rubber
- HNBR hydrogenated nitrile rubber
- SBR styrene-butadiene rubber
- EPDM ethylene propylene diene monomer rubber
- PEEK polyetheretherketone
- polyamide polyimide
- polysulfone polyester
- coated polymeric particles such as coated recycled rubber can effectively consolidate formation fines and/or filter fines out of the desired production material, minimizing or avoiding the problems associated with fines migration.
- coated polymeric particles can form a fluid- permeable pack which is effective in reducing or substantially preventing the passage of formation particles from the subterranean formation into a wellbore while allowing passage of formation fluids from the subterranean formation into the wellbore.
- the coated polymeric particles can be introduced into the subterranean formation through a treatment fluid during a downhole operation such as a hydraulic fracturing operation; an acidizing treatment; a gravel packing operation; a flooding operation; or a combination comprising at least one of the foregoing.
- a treatment fluid such as a hydraulic fracturing operation; an acidizing treatment; a gravel packing operation; a flooding operation; or a combination comprising at least one of the foregoing.
- the treatment fluid can be fracturing fluids, gravel packing fluids, flooding fluids, acidizing fluids, and the like.
- the treatment fluids can contain various components known in the art.
- fracturing fluids can contain proppant particles.
- Gravel packing fluids can contain gravels.
- Acidizing fluids contain an acid such as hydrofluoric acid; hydrochloric acid; acetic acid; formic acid; sulfamic acid; or chloroacetic acid.
- performing the downhole operation precedes introducing the treatment fluid.
- the treatment fluid containing the coated polymeric particles can be free of proppant particles, gravels, acids, or other components that may be needed for performing fracturing, gravel packing, acidizing, or flooding operations.
- the coated polymeric particles in the treatment fluids comprise a polymeric core and a curable coating disposed on the polymeric core.
- the polymeric core can be a rubber, such as a nitrile rubber (NBR), hydrogenated nitrile rubber (HNBR), styrene-butadiene rubber (SBR), ethylene propylene diene monomer rubber (EPDM), natural rubber, silicone rubber, polybutadiene, polyisoprene, butyl rubber, or a combination comprising at least one of the foregoing.
- NBR nitrile rubber
- HNBR hydrogenated nitrile rubber
- SBR styrene-butadiene rubber
- EPDM ethylene propylene diene monomer rubber
- natural rubber silicone rubber
- polybutadiene polyisoprene
- butyl rubber or a combination comprising at least one of the foregoing.
- the polymeric core can also be thermosets such as epoxy, phenolic, and the like or thermoplastics such as polyetheretherketone (PEEK), polyimide, polysulfone, polycarbonate, or a combination comprising at least one of the foregoing.
- thermosets such as epoxy, phenolic, and the like or thermoplastics such as polyetheretherketone (PEEK), polyimide, polysulfone, polycarbonate, or a combination comprising at least one of the foregoing.
- PEEK polyetheretherketone
- polyimide polyimide
- polysulfone polysulfone
- polycarbonate polycarbonate
- the polymeric core can be a recycled thermoset such as a recycled rubber, a recycled thermoplastic material, or a combination thereof.
- the recycled materials are environmentally friendly and low cost. The inventors have found that the particular recycled polymeric materials as disclosed herein can meet the requirements for the polymeric core in the context of sand control applications.
- Particularly preferred polymeric core is recycled rubber in a particulate form.
- recycled rubber refers to a rubber produced from used rubber products such as used tires. Recycled rubber can be made by pulverizing discarded rubber products at room temperature. Recycled rubber can also be made via a cryogenic process where the used rubber products are frozen to a cryogenic temperature then broken into particles or small pieces. The recycled rubber can have a particle size of about 3.5 to about 40 mesh.
- the polymeric core a curable coating, which cures subsurface, e.g. downhole or in a fracture.
- a curable coating means that the material for the coating can be polymerized or crosslinked, preferably under downhole conditions.
- thermoset coating includes uncured or partially cured thermosets such as epoxy resin, phenolic resin, vinyl ester resin, furan resin, polyurethane, polyester, cyanate ester, polyimide, bismaleimide, liquid rubber or a combination comprising at least one of the foregoing.
- the coating includes a curing agent.
- the curing agent can be nitrogen-containing compounds such as amines and their derivatives; oxygen-containing compounds such as carboxylic acid terminated polyesters, anhydrides, phenol-formaldehyde resins, amino-formaldehyde resins, phenol, bisphenol A and cresol novolacs, phenolic- terminated epoxy resins; elemental sulfur, sulfur-containing compounds such as polysulfides, polymercaptans; peroxides; catalytic curing agents such as tertiary amines, Lewis acids, Lewis bases; or a combination thereof.
- the coating is disposed on the polymeric core by mixing in a vessel, e.g., a reactor.
- a vessel e.g., a reactor.
- Individual components e.g., the polymeric core and resin materials (e.g., monomers and/or oligomers used to form a curable thermoset coating) are combined in the vessel to form a reaction mixture and are agitated to mix the components. Further, the reaction mixture is heated at a temperature or at a pressure commensurate with forming the coating.
- the coating is disposed on the polymeric core via spraying such as by contacting the polymeric core with a spray of the coating material.
- the coated polymeric particles have a size from about 50 pm to about 8,000 pm, specifically about 100 pm to about 7,000 pm, and more specifically about 1,000 pm to about 7,000 pm. Further, the coated polymeric particles have any shape including spherical, angular, and polyhedral and are monodisperse or polydisperse with an average particle size distribution that is unimodal or multimodal, e.g., bimodal.
- the thickness of the curable thermoset coating can be about 5 pm to about 500 pm or about 10 pm to about 50 pm.
- the coated polymeric particles are lightweight and can be conveniently injected downhole together with a carrier fluid.
- the coated polymeric particles have a true specific gravity of less than about 2 g/cc or about 0.5 g/cc to about 1.5 g/cc.
- coated polymeric particles as disclosed herein are stable at temperatures of up to about 350°F or up to about 300°F, thus providing a broader service temperature range compared to shape memory polymers.
- the coated polymeric particles are present in an amount effective to form a permeable pack in about 10 minutes to about 48 hours, about 30 minutes to about 36 hours, about 1 hour to about 24 hours, or about 2 hours to about 20 hours after injected into the wellbore.
- the treatment fluids can contain about 0.5 to about 10 lb/gal, or about 1 to about 5 lb/gal of the coated polymeric particles.
- the coated polymeric particles are used together with coated or uncoated proppants.
- the coating for the proppant can be the same as the coating for the coated polymeric particles.
- the proppant particles include a ceramic, sand, a mineral, a nut shell, gravel, glass, or a combination thereof.
- the ceramic include an oxide- based ceramic, nitride-based ceramic, carbide-based ceramic, boride-based ceramic, silicide- based ceramic, or a combination thereof.
- the oxide-based ceramic is silica (S1O2), titania (T1O2), aluminum oxide, boron oxide, potassium oxide, zirconium oxide, magnesium oxide, calcium oxide, lithium oxide, phosphorous oxide, and/or titanium oxide, or a combination thereof.
- the oxide-based ceramic, nitride-based ceramic, carbide-based ceramic, boride-based ceramic, or silicide-based ceramic contain a nonmetal (e.g., oxygen, nitrogen, boron, carbon, or silicon, and the like), metal (e.g., aluminum, lead, bismuth, and the like), transition metal (e.g., niobium, tungsten, titanium, zirconium, hafnium, yttrium, and the like), alkali metal (e.g., lithium, potassium, and the like), alkaline earth metal (e.g., calcium, magnesium, strontium, and the like), rare earth (e.g., lanthanum, cerium, and the like), or halogen (e.g., fluorine, chlorine, and the like).
- a nonmetal e.g., oxygen, nitrogen, boron, carbon, or silicon, and the like
- metal e.g., aluminum, lead, bismuth, and the like
- Exemplary ceramics include zirconia, stabilized zirconia, mullite, zirconia toughened alumina, spinel, aluminosilicates (e.g., mullite, cordierite), perovskite, silicon carbide, silicon nitride, titanium carbide, titanium nitride, aluminum carbide, aluminum nitride, zirconium carbide, zirconium nitride, iron carbide, aluminum oxynitride, silicon aluminum oxynitride, aluminum titanate, tungsten carbide, tungsten nitride, steatite, and the like, or a combination thereof.
- aluminosilicates e.g., mullite, cordierite
- perovskite silicon carbide, silicon nitride, titanium carbide, titanium nitride, aluminum carbide, aluminum nitride, zirconium carbide, zirconium nitride, iron carbide, aluminum
- Suitable sands for the proppant particles include, but are not limited to, Arizona sand, Wisconsin sand, Badger sand, Brady sand, and Ottawa sand.
- the proppant particles made of a mineral such as bauxite are sintered to obtain a hard material.
- the bauxite or sintered bauxite has a relatively high permeability such as the bauxite material disclosed in US Patent No. 4,713,203, the content of which is incorporated by reference herein in its entirety.
- Naturally occurring proppant particles include nut shells such as walnut, coconut, pecan, almond, ivory nut, brazil nut, and the like; seed shells of fruits such as plum, olive, peach, cherry, apricot, and the like; seed shells of other plants such as maize (e.g., corn cobs or corn kernels); wood materials such as those derived from oak, hickory, walnut, poplar, mahogany, and the like. Such materials are particles formed by crushing, grinding, cutting, chipping, and the like.
- the weight ratio of the coated polymeric particles relative to the proppant is about 10:90 to about 90: 10 or about 30:70 to about 70:30.
- the coated polymeric particles are not used together with any proppant.
- the treatment fluids that contain the coated thermoset can be free of proppants, coated or uncoated.
- the treatment fluids can further comprise an aqueous carrier fluid.
- the aqueous carrier fluid is present in an amount of about 10% to about 99% by weight, more specifically in an amount of about 20% to about 99% by weight, based on the total weight of the treatment fluids depending on the end use of the fluid.
- the aqueous carrier fluid can be fresh water, brine (including seawater), an aqueous base, or a combination comprising at least one of the foregoing. It will be appreciated that other polar liquids such as alcohols and glycols, alone or together with water, can be used in the carrier fluid.
- the brine can be, for example, seawater, produced water, completion brine, or a combination comprising at least one of the foregoing.
- the properties of the brine can depend on the identity and components of the brine.
- Seawater for example, can contain numerous constituents including sulfate, bromine, and trace metals, beyond typical halide- containing salts.
- Produced water can be water extracted from a production reservoir (e.g., hydrocarbon reservoir) or produced from an underground reservoir source of fresh water or brackish water. Produced water can also be referred to as reservoir brine and contain components including barium, strontium, and heavy metals.
- completion brine can be synthesized from fresh water by addition of various salts for example, KC1, NaCl, ZnCb, MgCb, or CaCb to increase the density of the brine, such as 10.6 pounds per gallon of CaCb brine.
- various salts for example, KC1, NaCl, ZnCb, MgCb, or CaCb to increase the density of the brine, such as 10.6 pounds per gallon of CaCb brine.
- Completion brines typically provide a hydrostatic pressure optimized to counter the reservoir pressures downhole.
- the above brines can be modified to include one or more additional salts.
- the additional salts included in the brine can be NaCl, KC1, NaBr, MgCb, CaCb, CaBr 2 , ZnBr 2 , NH4CI, sodium formate, cesium formate, and combinations comprising at least one of the foregoing.
- the NaCl salt can be present in the brine in an amount of about 0.5 to about 25 weight percent (wt.%), specifically about 1 to about 15 wt.%, and more specifically about 3 to about 10 wt.%, based on the weight of the brine.
- the aqueous carrier fluid of the treatment fluids can be foamed with a liquid hydrocarbon or a gas or liquefied gas such as nitrogen, or air.
- the fluid can further be foamed by inclusion of a non-gaseous foaming agent.
- the non-gaseous foaming agent can be amphoteric, cationic, or anionic. Suitable amphoteric foaming agents include alkyl betaines, alkyl sultaines, and alkyl carboxylates.
- Suitable anionic foaming agents can include alkyl ether sulfates, ethoxylated ether sulfates, phosphate esters, alkyl ether phosphates, ethoxylated alcohol phosphate esters, alkyl sulfates, and alpha olefin sulfonates.
- Suitable cationic foaming agents can include alkyl quaternary ammonium salts, alkyl benzyl quaternary ammonium salts, and alkyl amido amine quaternary ammonium salts.
- a foam system is mainly used in low pressure or water sensitive formations.
- a mixture of foaming and foam stabilizing dispersants can be used. Generally, the mixture can be included in the treatment fluids in an amount of about 1% to about 5% by volume of water in the treatment fluids.
- the various treatment fluids can be varied and adjusted according to well control and compatibility parameters of the particular fluid with which it is associated for example a fracturing fluid, an acidizing fluid, and the like.
- the treatment fluids can be used to reduce or substantially prevent the migration of fines in the subterranean formation and can be used in vertical, horizontal, or deviated wellbores.
- the components of the treatment fluids can be premixed or is injected into the wellbore without mixing, e.g., injected“on the fly” where the components are combined as they are being injected downhole.
- a pumpable or pourable treatment fluid can be formed by any suitable method.
- the components of the treatment fluid are combined using conventional mixing equipment or equipment used in downhole operations.
- the treatment fluid can then be injected, e.g., pumped and placed by various conventional pumps and tools to any desired location within the wellbore.
- injecting the treatment fluid comprises pumping the fluid via a tubular in the wellbore.
- the treatment fluid can be pumped into an annulus between a tubular and a wall of the wellbore via the tubular.
- the curable coating on the coated polymeric particles is cured.
- the coated polymeric particles are consolidated forming a fluid-permeable pack.
- the fluid-permeable pack reduces or substantially prevents the passage of formation particles from the subterranean formation into the wellbore while allowing passage of formation fluids from the subterranean formation into the wellbore.
- a method of reducing fines migration thus comprises introducing into the subterranean formation a treatment fluid comprising coated polymeric particles; curing the coating on these polymeric particles, and consolidating coated polymeric particles forming the fluid-permeable pack.
- the permeability of the fluid-permeable pack can be controlled by turning the particle size of the coated polymeric particles, the material of the coating, as well as the thickness of the coating.
- the fluid-permeable pack is effective in reducing or substantially preventing the passage of formation particles such as formation fines from the subterranean formation into a wellbore while allowing passage of formation fluids from the subterranean formation into the wellbore.
- the coated polymeric particles When used in hydraulic fracturing, the coated polymeric particles may be injected into a subterranean formation in conjunction with a hydraulic fracturing treatment or other treatment at pressures sufficiently high enough to cause the formation or enlargement of fractures.
- Such other treatments may be near wellbore in nature (affecting near wellbore regions) and may be directed toward improving wellbore productivity and/or controlling the production of fracture proppant or formation sand.
- Particular examples include gravel packing and "frac-packs.”
- a treatment fluid containing coated polymeric particles can be introduced into the subterranean formation to form a fluid-permeable pack, which reduces or substantially preventing the passage of formation particles from the subterranean formation into the wellbore while allowing passage of formation fluids from the subterranean formation into the wellbore.
- a gravel packing operation may be carried out on a wellbore that penetrates a subterranean formation to prevent or substantially reduce the production of formation particles into the wellbore from the formation during production of formation fluids.
- the subterranean formation may be completed so as to be in
- a screen assembly such as is known in the art may be placed or otherwise disposed within the wellbore so that at least a portion of the screen assembly is disposed adjacent the subterranean formation.
- a treatment fluid including the coated polymeric particles may then be introduced into the wellbore and placed adjacent the subterranean formation by circulation or other suitable method so as to form a fluid-permeable pack in an annular area between the exterior of the screen and the interior of the wellbore that is capable of reducing or substantially preventing the passage of formation particles from the subterranean formation into the wellbore during production of fluids from the formation, while at the same time allowing passage of formation fluids from the subterranean formation through the screen into the wellbore.
- the fines migration control method may use the coated polymeric particles in accordance with any method in which a pack of particulate material is formed within a wellbore that it is permeable to fluids produced from a wellbore, such as oil, gas, or water, but that substantially prevents or reduces production of formation materials, such as formation sand, from the formation into the wellbore.
- a pack of particulate material is formed within a wellbore that it is permeable to fluids produced from a wellbore, such as oil, gas, or water, but that substantially prevents or reduces production of formation materials, such as formation sand, from the formation into the wellbore.
- Such methods may or may not employ a gravel packing screen, may be introduced into a wellbore at pressures below, at or above the fracturing pressure of the formation, such as frac pack, and/or may be employed in conjunction with resins such as sand consolidation resins if so desired.
- Embodiment 1 A method of treating a subterranean formation penetrated by a wellbore, the method comprising: introducing into the subterranean formation a treatment fluid comprising coated polymeric particles having a polymeric core and a curable thermoset coating disposed on the polymeric core, the polymeric core comprising a rubber, an epoxy, a phenolic resin, a thermoplastic polymer or a combination comprising at least one of the foregoing, the rubber comprising a nitrile rubber (NBR), a hydrogenated nitrile rubber (HNBR), a styrene-butadiene rubber (SBR), an ethylene propylene diene monomer rubber (EPDM), a natural rubber, a silicone rubber, a polybutadiene, polyisoprene, butyl rubber, or a combination comprising at least one of the foregoing, and the thermoplastic polymer comprising polyetheretherketone (PEEK), a polyimide, a polysulfon-
- Embodiment 2 The method as in any prior embodiment, wherein the polymeric core is a recycled polymeric material.
- Embodiment 3 The method as in any prior embodiment, wherein the polymeric core is a recycled rubber in a particulate form.
- the recycled rubber has a size of about 3.5 to about 40 mesh.
- Embodiment 4 The method as in any prior embodiment, wherein the curable thermoset coating comprises an uncured or partially cured thermoset including an epoxy resin, a phenolic resin, a vinyl ester resin, a furan resin, a polyurethane, a polyester, a cyanate ester, a polyimide, a bismaleimide, a liquid rubber or a combination comprising at least one of the foregoing.
- an epoxy resin a phenolic resin, a vinyl ester resin, a furan resin, a polyurethane, a polyester, a cyanate ester, a polyimide, a bismaleimide, a liquid rubber or a combination comprising at least one of the foregoing.
- Embodiment 5 The method as in any prior embodiment, wherein the curable thermoset coating further comprises a curing agent.
- the curing agent can include an amine, an oxygen-containing compound, elemental sulfur, a sulfur-containing compound, a peroxide, a Lewis acid, a Lewis base; or a combination comprising at least one of the foregoing.
- Embodiment 6 The method as in any prior embodiment, wherein the coated polymeric particles have an average particle size of about 1,000 pm to about 7,000 pm.
- Embodiment 7 The method as in any prior embodiment, wherein the treatment fluid further comprises a proppant.
- the proppant can comprise an uncoated proppant, a coated proppant, or a combination thereof.
- the weight ratio of the coated polymeric particles relative to the proppant can be about 10:90 to about 90: 10.
- Embodiment 8 The method as in any prior embodiment, wherein the forming the fluid-permeable pack comprises consolidating the coated polymeric particles with the coating during curing.
- Embodiment 9 The method as in any prior embodiment, further comprising performing a downhole operation comprising one or more of the following: a hydraulic fracturing operation; an acidizing treatment; a gravel packing operation; or a flooding operation. Introducing the treatment fluid and the performing the downhole operation can occur simultaneously. Alternatively, performing the downhole operation precedes introducing the treatment fluid.
- Embodiment 10 The method as in any prior embodiment, further comprising adjusting the permeability of the fluid-permeable pack by changing the size of the coated polymeric particles, the thickness of the curable thermoset coating, a composition of the curable thermoset coating, or a combination thereof.
- Embodiment 11 The method as in any prior embodiment, wherein the fluid- permeable pack is disposed adjacent the subterranean formation.
- Embodiment 12 The method as in any prior embodiment, wherein the fluid- permeable pack is disposed in a fracture created by a hydraulic fracturing operation.
- Embodiment 13 The method as in any prior embodiment, further comprising installing a screen device in the wellbore.
- the fluid-permeable pack can be disposed in an annular area between the exterior of the screen device and the interior of the wellbore.
- Embodiment 14 Coated polymeric particles comprising: a recycled polymeric core in a particulate form, and a curable coating disposed on the polymeric core, wherein recycled polymeric core has a size of about 3.5 to 40 mesh and comprises nitrile rubber (NBR), hydrogenated nitrile rubber (HNBR), styrene-butadiene rubber (SBR), ethylene propylene diene monomer rubber (EPDM), natural rubber, silicone rubber, polybutadiene, polyisoprene, butyl rubber, rubber blend, polyetheretherketone (PEEK), polyamide, polyimide, polysulfone, polyester, polycarbonate, or a combination comprising at least one of the foregoing.
- NBR nitrile rubber
- HNBR hydrogenated nitrile rubber
- SBR styrene-butadiene rubber
- EPDM ethylene propylene diene monomer rubber
- PEEK polyetheretherketone
- polyamide polyimide
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- Environmental & Geological Engineering (AREA)
- Chemical Kinetics & Catalysis (AREA)
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Abstract
Description
Claims
Priority Applications (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB2100777.8A GB2590249B (en) | 2018-06-28 | 2019-05-29 | Methods of controlling fines migration in a well |
| AU2019292056A AU2019292056A1 (en) | 2018-06-28 | 2019-05-29 | Methods of controlling fines migration in a well |
| NO20210019A NO20210019A1 (en) | 2018-06-28 | 2021-01-07 | Methods of controlling fines migration in a well |
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US16/021,142 | 2018-06-28 | ||
| US16/021,142 US10767101B2 (en) | 2018-06-28 | 2018-06-28 | Methods of controlling fines migration in a well |
Publications (1)
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| WO2020005443A1 true WO2020005443A1 (en) | 2020-01-02 |
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|---|---|---|---|
| PCT/US2019/034338 Ceased WO2020005443A1 (en) | 2018-06-28 | 2019-05-29 | Methods of controlling fines migration in a well |
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| US (1) | US10767101B2 (en) |
| AU (1) | AU2019292056A1 (en) |
| GB (1) | GB2590249B (en) |
| NO (1) | NO20210019A1 (en) |
| WO (1) | WO2020005443A1 (en) |
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US12365828B2 (en) | 2021-05-11 | 2025-07-22 | ExxonMobil Technology and Engineering Company | Polyolefin-coke composite granules as a hydraulic fracturing proppant |
| US12466992B2 (en) | 2022-03-04 | 2025-11-11 | ExxonMobil Technology and Engineering Company | Proppants derived from crosslinking mixed aromatic resins |
| CN117089335B (en) * | 2022-05-13 | 2025-02-25 | 中国石油天然气股份有限公司 | Expansion material and preparation method and application thereof |
| US12540273B2 (en) | 2024-01-19 | 2026-02-03 | ExxonMobil Technology and Engineering Company | Proppant particles formed from fluid coke and flexicoke, fracturing fluids comprising such proppant particles, and methods related thereto |
| US12521764B2 (en) | 2024-06-19 | 2026-01-13 | ExxonMobil Technology and Engineering Company | Methods for preparing petroleum coke proppant particles for hydraulic fracturing |
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| US20050019574A1 (en) * | 2003-04-15 | 2005-01-27 | Mccrary Avis Lloyd | Particulate material containing thermoplastics and methods for making and using the same |
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| WO2017048230A1 (en) * | 2015-09-15 | 2017-03-23 | Halliburton Energy Services, Inc. | Core-shell particles for treatment of subterranean formations |
| WO2017151699A1 (en) * | 2016-03-02 | 2017-09-08 | Baker Hughes Incorporated | Methods of controlling fines migration in a well |
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| US4713203A (en) | 1985-05-23 | 1987-12-15 | Comalco Aluminium Limited | Bauxite proppant |
| US6749025B1 (en) | 1996-11-27 | 2004-06-15 | Bj Services Company | Lightweight methods and compositions for sand control |
| US6582819B2 (en) * | 1998-07-22 | 2003-06-24 | Borden Chemical, Inc. | Low density composite proppant, filtration media, gravel packing media, and sports field media, and methods for making and using same |
| US7244492B2 (en) * | 2004-03-04 | 2007-07-17 | Fairmount Minerals, Ltd. | Soluble fibers for use in resin coated proppant |
| US8227026B2 (en) * | 2004-09-20 | 2012-07-24 | Momentive Specialty Chemicals Inc. | Particles for use as proppants or in gravel packs, methods for making and using the same |
| US7931087B2 (en) | 2006-03-08 | 2011-04-26 | Baker Hughes Incorporated | Method of fracturing using lightweight polyamide particulates |
| CA2849755C (en) * | 2011-09-30 | 2017-04-11 | Momentive Specialty Chemicals Inc. | Proppant materials and methods of tailoring proppant material surface wettability |
| US20190031950A1 (en) * | 2013-10-30 | 2019-01-31 | Baker Hughes, A Ge Company, Llc | Method of enhancing conductivity in a subterranean formation |
| US10017688B1 (en) * | 2014-07-25 | 2018-07-10 | Hexion Inc. | Resin coated proppants for water-reducing application |
| WO2016044016A1 (en) * | 2014-09-16 | 2016-03-24 | Durez Corporation | Low temperature curable proppant |
-
2018
- 2018-06-28 US US16/021,142 patent/US10767101B2/en active Active
-
2019
- 2019-05-29 GB GB2100777.8A patent/GB2590249B/en active Active
- 2019-05-29 AU AU2019292056A patent/AU2019292056A1/en not_active Abandoned
- 2019-05-29 WO PCT/US2019/034338 patent/WO2020005443A1/en not_active Ceased
-
2021
- 2021-01-07 NO NO20210019A patent/NO20210019A1/en unknown
Patent Citations (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US20050019574A1 (en) * | 2003-04-15 | 2005-01-27 | Mccrary Avis Lloyd | Particulate material containing thermoplastics and methods for making and using the same |
| US20110253366A1 (en) * | 2008-12-23 | 2011-10-20 | Berrigan Michael R | Curable fiber |
| US20150203744A1 (en) * | 2014-01-22 | 2015-07-23 | Sumitomo Bakelite Co., Ltd. | Resin composition, coated particles, injection material and method for injecting injection material into fracture |
| WO2017048230A1 (en) * | 2015-09-15 | 2017-03-23 | Halliburton Energy Services, Inc. | Core-shell particles for treatment of subterranean formations |
| WO2017151699A1 (en) * | 2016-03-02 | 2017-09-08 | Baker Hughes Incorporated | Methods of controlling fines migration in a well |
Also Published As
| Publication number | Publication date |
|---|---|
| GB2590249B (en) | 2022-12-14 |
| NO20210019A1 (en) | 2021-01-07 |
| US20200002601A1 (en) | 2020-01-02 |
| GB202100777D0 (en) | 2021-03-03 |
| US10767101B2 (en) | 2020-09-08 |
| GB2590249A (en) | 2021-06-23 |
| AU2019292056A1 (en) | 2021-02-04 |
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