WO2009085112A2 - Nano particle reinforced polymer element for a stator and rotor assembly - Google Patents
Nano particle reinforced polymer element for a stator and rotor assembly Download PDFInfo
- Publication number
- WO2009085112A2 WO2009085112A2 PCT/US2008/013571 US2008013571W WO2009085112A2 WO 2009085112 A2 WO2009085112 A2 WO 2009085112A2 US 2008013571 W US2008013571 W US 2008013571W WO 2009085112 A2 WO2009085112 A2 WO 2009085112A2
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- stator
- rotor assembly
- recited
- rotor
- cavity
- Prior art date
Links
- 229920000642 polymer Polymers 0.000 title claims abstract description 146
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- NBVXSUQYWXRMNV-UHFFFAOYSA-N fluoromethane Chemical compound FC NBVXSUQYWXRMNV-UHFFFAOYSA-N 0.000 claims 1
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- 239000005995 Aluminium silicate Substances 0.000 description 1
- 240000008100 Brassica rapa Species 0.000 description 1
- 229910052684 Cerium Inorganic materials 0.000 description 1
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- 229910019142 PO4 Inorganic materials 0.000 description 1
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical group [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 1
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 1
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- 125000003342 alkenyl group Chemical group 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 235000012211 aluminium silicate Nutrition 0.000 description 1
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- 229960000892 attapulgite Drugs 0.000 description 1
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- 229910000278 bentonite Inorganic materials 0.000 description 1
- SVPXDRXYRYOSEX-UHFFFAOYSA-N bentoquatam Chemical compound O.O=[Si]=O.O=[Al]O[Al]=O SVPXDRXYRYOSEX-UHFFFAOYSA-N 0.000 description 1
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- ZMIGMASIKSOYAM-UHFFFAOYSA-N cerium Chemical compound [Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce][Ce] ZMIGMASIKSOYAM-UHFFFAOYSA-N 0.000 description 1
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- GUJOJGAPFQRJSV-UHFFFAOYSA-N dialuminum;dioxosilane;oxygen(2-);hydrate Chemical compound O.[O-2].[O-2].[O-2].[Al+3].[Al+3].O=[Si]=O.O=[Si]=O.O=[Si]=O.O=[Si]=O GUJOJGAPFQRJSV-UHFFFAOYSA-N 0.000 description 1
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- 125000005843 halogen group Chemical group 0.000 description 1
- 230000020169 heat generation Effects 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- KWLMIXQRALPRBC-UHFFFAOYSA-L hectorite Chemical compound [Li+].[OH-].[OH-].[Na+].[Mg+2].O1[Si]2([O-])O[Si]1([O-])O[Si]([O-])(O1)O[Si]1([O-])O2 KWLMIXQRALPRBC-UHFFFAOYSA-L 0.000 description 1
- 229910000271 hectorite Inorganic materials 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 1
- 229910052900 illite Inorganic materials 0.000 description 1
- RHZWSUVWRRXEJF-UHFFFAOYSA-N indium tin Chemical compound [In].[Sn] RHZWSUVWRRXEJF-UHFFFAOYSA-N 0.000 description 1
- 125000001905 inorganic group Chemical group 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 1
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- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 1
- VGIBGUSAECPPNB-UHFFFAOYSA-L nonaaluminum;magnesium;tripotassium;1,3-dioxido-2,4,5-trioxa-1,3-disilabicyclo[1.1.1]pentane;iron(2+);oxygen(2-);fluoride;hydroxide Chemical compound [OH-].[O-2].[O-2].[O-2].[O-2].[O-2].[F-].[Mg+2].[Al+3].[Al+3].[Al+3].[Al+3].[Al+3].[Al+3].[Al+3].[Al+3].[Al+3].[K+].[K+].[K+].[Fe+2].O1[Si]2([O-])O[Si]1([O-])O2.O1[Si]2([O-])O[Si]1([O-])O2.O1[Si]2([O-])O[Si]1([O-])O2.O1[Si]2([O-])O[Si]1([O-])O2.O1[Si]2([O-])O[Si]1([O-])O2.O1[Si]2([O-])O[Si]1([O-])O2.O1[Si]2([O-])O[Si]1([O-])O2 VGIBGUSAECPPNB-UHFFFAOYSA-L 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- 229910052625 palygorskite Inorganic materials 0.000 description 1
- 235000021317 phosphate Nutrition 0.000 description 1
- 125000002467 phosphate group Chemical class [H]OP(=O)(O[H])O[*] 0.000 description 1
- 229910052698 phosphorus Inorganic materials 0.000 description 1
- 239000011574 phosphorus Chemical group 0.000 description 1
- 239000004014 plasticizer Substances 0.000 description 1
- 239000011148 porous material Substances 0.000 description 1
- 230000002028 premature Effects 0.000 description 1
- 238000011084 recovery Methods 0.000 description 1
- 239000012779 reinforcing material Substances 0.000 description 1
- 230000003252 repetitive effect Effects 0.000 description 1
- 150000004819 silanols Chemical class 0.000 description 1
- 239000002210 silicon-based material Substances 0.000 description 1
- HPALAKNZSZLMCH-UHFFFAOYSA-M sodium;chloride;hydrate Chemical compound O.[Na+].[Cl-] HPALAKNZSZLMCH-UHFFFAOYSA-M 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- 239000002344 surface layer Substances 0.000 description 1
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- 230000002277 temperature effect Effects 0.000 description 1
- 239000010936 titanium Substances 0.000 description 1
- 229910052719 titanium Inorganic materials 0.000 description 1
- 230000003313 weakening effect Effects 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
- 229910052726 zirconium Inorganic materials 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K9/00—Use of pretreated ingredients
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K3/00—Use of inorganic substances as compounding ingredients
- C08K3/02—Elements
- C08K3/04—Carbon
- C08K3/041—Carbon nanotubes
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/54—Silicon-containing compounds
- C08K5/549—Silicon-containing compounds containing silicon in a ring
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K7/00—Use of ingredients characterised by shape
- C08K7/22—Expanded, porous or hollow particles
- C08K7/24—Expanded, porous or hollow particles inorganic
-
- 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
- E21B4/00—Drives for drilling, used in the borehole
- E21B4/02—Fluid rotary type drives
-
- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F01—MACHINES OR ENGINES IN GENERAL; ENGINE PLANTS IN GENERAL; STEAM ENGINES
- F01C—ROTARY-PISTON OR OSCILLATING-PISTON MACHINES OR ENGINES
- F01C1/00—Rotary-piston machines or engines
- F01C1/08—Rotary-piston machines or engines of intermeshing engagement type, i.e. with engagement of co- operating members similar to that of toothed gearing
- F01C1/10—Rotary-piston machines or engines of intermeshing engagement type, i.e. with engagement of co- operating members similar to that of toothed gearing of internal-axis type with the outer member having more teeth or tooth-equivalents, e.g. rollers, than the inner member
- F01C1/107—Rotary-piston machines or engines of intermeshing engagement type, i.e. with engagement of co- operating members similar to that of toothed gearing of internal-axis type with the outer member having more teeth or tooth-equivalents, e.g. rollers, than the inner member with helical teeth
-
- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F04—POSITIVE - DISPLACEMENT MACHINES FOR LIQUIDS; PUMPS FOR LIQUIDS OR ELASTIC FLUIDS
- F04C—ROTARY-PISTON, OR OSCILLATING-PISTON, POSITIVE-DISPLACEMENT MACHINES FOR LIQUIDS; ROTARY-PISTON, OR OSCILLATING-PISTON, POSITIVE-DISPLACEMENT PUMPS
- F04C15/00—Component parts, details or accessories of machines, pumps or pumping installations, not provided for in groups F04C2/00 - F04C14/00
- F04C15/0003—Sealing arrangements in rotary-piston machines or pumps
- F04C15/0007—Radial sealings for working fluid
- F04C15/0015—Radial sealings for working fluid of resilient material
-
- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F04—POSITIVE - DISPLACEMENT MACHINES FOR LIQUIDS; PUMPS FOR LIQUIDS OR ELASTIC FLUIDS
- F04C—ROTARY-PISTON, OR OSCILLATING-PISTON, POSITIVE-DISPLACEMENT MACHINES FOR LIQUIDS; ROTARY-PISTON, OR OSCILLATING-PISTON, POSITIVE-DISPLACEMENT PUMPS
- F04C2/00—Rotary-piston machines or pumps
- F04C2/08—Rotary-piston machines or pumps of intermeshing-engagement type, i.e. with engagement of co-operating members similar to that of toothed gearing
- F04C2/10—Rotary-piston machines or pumps of intermeshing-engagement type, i.e. with engagement of co-operating members similar to that of toothed gearing of internal-axis type with the outer member having more teeth or tooth-equivalents, e.g. rollers, than the inner member
- F04C2/107—Rotary-piston machines or pumps of intermeshing-engagement type, i.e. with engagement of co-operating members similar to that of toothed gearing of internal-axis type with the outer member having more teeth or tooth-equivalents, e.g. rollers, than the inner member with helical teeth
- F04C2/1071—Rotary-piston machines or pumps of intermeshing-engagement type, i.e. with engagement of co-operating members similar to that of toothed gearing of internal-axis type with the outer member having more teeth or tooth-equivalents, e.g. rollers, than the inner member with helical teeth the inner and outer member having a different number of threads and one of the two being made of elastic materials, e.g. Moineau type
Definitions
- This invention relates, in general, to a polymer element of a stator and rotor assembly for power sections of positive displacement downhole fluid motors and progressive cavity pumps and, in particular, to an improved polymer element of a stator or rotor element comprised of a nano particle reinforced polymer internally disposed in a stator lining or disposed as a uniform compliant layer along a rotor surface.
- a typical power section of a positive displacement fluid motor comprises a helical-shaped steel rotor that turns rotatably about the centerline of a polymer-lined stator and rotor assembly.
- a typical stator is a steel tube, lined with a bonded polymer with a helical-shaped inner cavity.
- High pressure fluid flows through the power section of the positive displacement fluid motor causing the rotor to turn rotatably within the stator.
- the positive displacement fluid motor converts the hydraulic energy of high pressure fluid to mechanical energy in the form of torque output at the rotor; for example, to turn a drill bit.
- the rotor is typically a steel helix with a circular cross section with a smooth hard surface for wear resistance.
- the rotor is disposed inside the stator and a plurality of cavities defined by a seal plane between the rotor and the helical curve of the polymer core of the stator.
- the seal plane between the rotor surface and the polymer lining of the stator rotates around the centerline of the stator, advancing the cavities lengthwise along the stator and rotor assembly.
- Each of the cavities is sealed from adjacent cavities by the seal plane.
- Slip of the power section occurs when high pressure fluid bypasses the interface between the rotor and the stator without producing a resultant rotational force in the rotor. Slip results in speed and power reduction of a power section until, at some point, the power section stalls, allowing substantially all fluid to bypass the interface between the rotor and the stator with no resultant rotation produced by the power section.
- Progressive cavity pumps also known as progressing cavity pumps or eccentric screw pumps, are typically comprised of a helical steel rotor that turns rotatably within a helical-shaped, polymer-lined stator.
- the rotor is typically turned by a mechanical means, such as a motor or subassembly of a drill string. As the rotor turns, the interface between the rotor and the stator rotates around the centerline of the stator, advancing the cavities lengthwise along the stator to force the contents of the cavities through the stages of the pump.
- a mechanical means such as a motor or subassembly of a drill string.
- Failure of the polymer element of a power section of a positive displacement fluid motor or a progressive cavity pump typically occurs due to high mechanical loading, polymer fatigue, incompatibility of the fluid and polymer, or high temperature effects on the polymer element. Failure may be associated with a reduction in the performance of the polymer element or with catastrophic failure.
- Excessive operating temperature may cause expansion of the polymer that increases the compressive interference between the rotor and the stator, further increasing hysteresis heat generation and wear.
- Certain chemicals may react with the polymer element of the stator and rotor assembly and cause degradation of the polymer or the bond between the polymer and the metal surface by weakening the molecular bonding of the polymer.
- synthetic oils or aromatic compounds found in drilling fluids and drilling fluids buffered with chemicals or composed of high alkalinity brine solutions may cause degradation of the polymer.
- Stators are typically manufactured by an injection molding process that introduces a relatively high viscosity, uncured polymer compound into an annular space between a mold and the inner wall of the stator housing. It is preferred that the polymer element of the stator lining is formed evenly and uniformly to avoid inconsistent thickness of the polymer that may cause excessive flexure of the rotor and excessive stress in the polymer.
- Uniform thickness of the polymer element of the stator may be difficult to achieve due to the length of the stator housing into which the uncured polymer is injected and the relatively high viscosity of the uncured polymer.
- stator and rotor assembly and the method of manufacturing the present invention are discussed in the context of a positive displacement fluid motor and a progressive cavity pump, it will be appreciated that the present invention is also applicable to other systems that require repetitive flexure of polymers.
- the present invention discloses a stator and rotor assembly of a power section of a positive displacement fluid motor or a progressive cavity pump that includes a polymer element wherein the polymer is a polymer matrix reinforced with nano-sized particles to create a nano composite material with improved mechanical, thermal, physical, chemical, and processing properties.
- the polymer element may be manufactured from a nano particle polymer composite that includes a polymer host and one or more of a plurality of nano-sized structures.
- Introduction of nano particles to the uncured polymer may improve the physical properties of the polymer by reducing processing viscosity, improving impact strength, improving stress relaxation resistance, improving compression set properties, increasing tear strength, reducing creep, increasing resistance to thermal and hysteresis failure, and improving resistance to chemical degradation of the polymer.
- the polymer host material may be polymers, including but not limited to, elastomers, thermosets, or thermoplastics.
- the polymer host material may be an elastomer, such as nitrile, a copolymer of acrylonitrile and butadiene (NBR), or carboxylated acrylonitrile butadiene (XNBR), or hydrogenated acrylonitrile butadiene (HNBR), commonly referred to as highly saturated nitrile (HSN), or carboxylated hydrogenated acrylonitrile butadiene (XHNBR), or hydrogenated carboxylated acrylonitrile butadiene (HXNBR).
- NBR acrylonitrile and butadiene
- XNBR carboxylated acrylonitrile butadiene
- HNBR hydrogenated acrylonitrile butadiene
- the polymer host material may be a flurocarbon (FKM), such as tetrafluoroethylene and propylene (FEPM), or perfluoroelastomer (FFKM).
- FKM flurocarbon
- FEPM tetrafluoroethylene and propylene
- FFKM perfluoroelastomer
- the polymer host material may also be polychloroprene rubber (CR), natural rubber (NR), polyether eurethane (EU), styrene butadiene rubber (SBR), ethylene propylene (EPR), or ethylene propylene diene (EPDM) or similar elastomers.
- CR polychloroprene rubber
- NR natural rubber
- EU polyether eurethane
- SBR styrene butadiene rubber
- EPR ethylene propylene
- EPDM ethylene propylene diene
- the polymer host material may be a thermoplastic, such as polyphenylene sulfide (PPS), polyetherketone-ketone (PEKK), polyetheretherketone (PEEK), polyetherketone (PEK), polytetrafluorethylene (PTFE) or polysulphones (PSU).
- PPS polyphenylene sulfide
- PEKK polyetherketone-ketone
- PEEK polyetheretherketone
- PEK polytetrafluorethylene
- PSU polysulphones
- the nano structures of the nano composite material may include nano-sized particles approximately 0.1 nanometers to approximately 500 nanometers in the smallest dimension. Nano structures may be from a variety of shapes, such as plates, spheres, cylinders, tubes, fibers, three- dimensional structures, linear molecules, molecular rings, branched molecules and crystalline, amorphous, or symmetric shapes.
- Nano particles maybe from a variety of materials, such as carbon, silica, calcium, calcium carbonate, inorganic clays, or minerals.
- the nano structures may be formed from materials, such as nano clays, carbon nano fibers, carbon nano tubes or nano arrays.
- the polymer host material and the nano structures may interact via interfacial interactions, such as co-polymerization, crystallization, van der Waals interactions, covalent bonds, ionic bonds, and cross-linking interactions.
- interfacial interactions may be improved by chemical functionalization of the nano particles.
- incorporación of nano particles in the polymer improves the particle reinforced polymer matrix by reducing processing viscosity, improving impact strength, improving stress relaxation resistance, improving compression set properties, increasing tear strength, increasing resistance to thermal and hysteresis, reducing heat buildup failure, increasing thermal conductivity, reducing creep, improving resilience and abrasion resistance, and improving resistance to chemical degradation of the polymer.
- Nano particle reinforced polymers generally require lesser amounts of filler material than traditional fillers to achieve comparable physical properties.
- the lesser amount of nano material required to reinforce a cured polymer has a concomitant effect of lowering the uncured viscosity of the polymer and thereby improving the ability to manufacture longer and thinner profiles of polymer stator elements and improving physical properties at elevated temperatures.
- the nano particle composite structures may be chemically functionalized to enhance the effective surface area of the composite structure and improve the availability of potential chemical reactions or catalysis sites for chemical functional groups on the nano composite structure and increase the interaction between the polymer matrix and the nano particles.
- the inner surface of the stator may be a helical curve-shaped surface with a plurality of lobes dispersed longitudinally along the inner surface of the stator
- the rotor may be a steel helix coated with a uniform layer of compliant polymer of sufficient thickness to hydraulically engage the helical curve-shaped surface of the stator.
- the present invention is directed to a method for forming a stator assembly of a power section of a positive displacement drill motor or a progressive cavity pump that comprises injection molding a nano particle reinforced polymer comprised of a polymer host material and one or more nano-sized structures into an annular area between a mold disposed inside a metal stator housing and the stator housing and curing the elastomer.
- the method comprises steps that include coating a rotor with a nano particle reinforced polymer layer of sufficient uniform thickness to hydraulically engage a helical curve- shaped surface of the stator housing.
- Figure 4 is a schematic illustration of a nano particle composite polymer material comprised of a polymer host material and interlinked nano particles according to an embodiment of the present invention
- Figure 5 is a schematic illustration of a nano particle composite polymer material comprised of a polymer host material and interlinked nano tubes or nano fibers according to an embodiment of the present invention
- Figure 6 is a schematic illustration of a single-wall carbon nano tube
- Figure 7 is a schematic illustration of a multi-wall carbon nano tube
- Figure 8 is a schematic illustration of a single- wall carbon nano tube imbedded in a polymer host material and interlinked nano particles according to an embodiment of the present invention
- Figure 9 is a schematic illustration of a nano particle composite polymer material comprising a polymer host material and a nanostructure according to an embodiment of the present invention.
- Figure 10 is a schematic illustration of a silicon-based nanostructure according to an embodiment of the present invention.
- Figure 11 is a schematic illustration of a silicon-based nanostructure according to an embodiment of the present invention.
- Figure 12 is a schematic illustration of a silicon-based nanostructure according to an embodiment of the present invention.
- Figure 13 is a schematic illustration of a silicon-based nanostructure according to an embodiment of the present invention.
- Figure 14 is a schematic illustration of a nano particle composite polymer material, including a polymer host material, a plurality of nanostructures and an additive according to an embodiment of the present invention.
- the present invention generally relates to a system and method of manufacture for an improved polymer element of a stator and rotor assembly.
- the system and method are useful, for example, with a variety of applications related to a power section of a positive displacement fluid motor or a progressive cavity pump or a fluid pulse generating device; for example, Halliburton' s Pulsonix Deep Wave technology.
- a system 25 is illustrated according to an embodiment of the present invention.
- a stator and rotor assembly 25 is comprised of a stator 20 comprising an external tubular member 21 having an internal core of a polymer material 22 molded therein to define an elongated annular space 23.
- the rotor 24 is formed of a rigid material, for example, metal, and is disposed axially within the annular space 23.
- the tubular member 21 may be a metal tube and the uncured polymer may be molded into the tubular member by utilizing a helical-shaped mold (not shown) that is extended through center of the tubular member 21 before the uncured polymer 22 is injected into the annular space 23 between the mold and the inner wall of the tubular member 21.
- the mold is subsequently removed from the annular space 23 after the polymer 22 is cured.
- the polymer may be cured by applying heat treatment or pressure or a combination.
- a cross section of a stator and rotor assembly 25 ' is illustrated according to an embodiment of the present invention.
- the rotor 24' maybe machined of metal with an elongated helical configuration.
- the outer surface of the rotor 24' is preferably polished and may even be coated with a friction-reducing surface to reduce the torque necessary to overcome friction between the polymer element 22 ' of the stator 20' and the rotor 24' which are in contact with one another with an interference fit.
- the annular space 23 ' in the stator 20' is a two-start helical thread which extends in the same direction as that of the thread of the rotor 24', wherein each thread of the two-start configuration has a pitch length double that of the rotor 24'.
- the rotor 24" may have a plurality of lobes 26" of quantity N and the polymer element 22" of the stator 20" may have a number N+l of threads forming the annular space 23" of the stator 20".
- the inner surface of the stator 20" may be a helical curve-shaped profile with a plurality of lobes 29" dispersed longitudinally along the inner surface of the stator 20".
- the rotor 24" may be bonded to an outer layer of compliant polymer 28" of sufficient uniform thickness to hydraulically engage the helical curve-shaped inner surface of the stator 20".
- stator and rotor assembly 25 function as a power section of a positive displacement mud motor and the output of the rotor 24 is affixed to a drive shaft (not shown) connected to a downhole well tool; for example, a drill bit (not shown).
- Conduits may be attached to opposite ends of the stator and rotor assembly 25, which conduits provide inlet and outlet ports for the pumped fluid.
- the diameter of the cross section of the annular space 23 of the stator 20 is the same or less than the diameter of the circular shape of the rotor 24, thus providing an interference fit between the inner surface of the stator polymer 22 and the outer surface of the rotor 24.
- the points of contact between the stator 20 and the rotor 24 there may be distortion of the polymer material 22 as the stator 20 engages with the rotor 24.
- the points of engagement trace the elongated path of the rotor 24 as it rotates and contacts the polymer material 22.
- the annular spaces 23 formed by the points of engagement between the rotor 24 and polymer material 22 move progressively toward an outlet end of the stator and rotor assembly 25 as the rotor 24 rotates relative to the stator 20.
- the points of engagement define a seal between the annular spaces 23. The more effective the seal between the rotor 24 and polymer material 22, the greater the differential pressure that may be achieved without stalling of the stator and rotor assembly 25; thereby producing a higher output torque.
- the stator and the rotor assembly 25 comprise a progressive cavity pump
- the rotor 24 is turned rotatably by a drive source (not shown), for example, a motor, and a fluid is pumped from stage to stage of the pump to an outlet by the progressing annular spaces 23 of the stator and rotor assembly 25.
- a drive source for example, a motor
- a fluid is pumped from stage to stage of the pump to an outlet by the progressing annular spaces 23 of the stator and rotor assembly 25.
- the more effective the seal between the rotor 24 and the polymer material 22 the greater the discharge pressure of the pump.
- the elastomers of the stator and rotor assembly 25 of the present invention are preferably formed from a polymer material that has improved properties for substantially recovering in shape and size after removal of a deforming force; that is, a polymer material that exhibits physical and mechanical properties relative to elastic memory and elastic recovery. Accordingly, elastomers of the stator and rotor assembly 25 of the present invention are preferably formed from a polymer material produced by a curing method that involves compounding or mixing a base polymer with filler additives or agents that reinforce the polymer and improve the physical and chemical properties of the cured polymer 22.
- the polymer material of the stator and rotor assembly 25 may be manufactured from a polymer composite that includes a polymer host reinforced with a plurality of nano-sized filler material.
- Introduction of nano-sized filler particles to the uncured polymer may improve the physical and chemical properties of the cured polymer by reducing improving impact strength, improving stress relaxation resistance, improving compression set properties, improving durability and modulus, increasing tear strength, reducing creep, increasing resistance to thermal and hysteresis failure and improving resistance to chemical degradation of the polymer.
- the filler material is generally a nano-sized material in the range from approximately 0.1 nanometers to approximately 500 nanometers, at the least dimension.
- Nano particle reinforced polymers generally require smaller amounts of filler material than traditional fillers to achieve comparable improvements in physical and chemical properties as compared to polymers with significantly larger particles or non-reinforced polymers.
- the smaller amount of nano material required to reinforce the elastomer has a concomitant effect of lowering the uncured viscosity of the elastomer thus improving the ability to form longer and thinner profiles of polymer elements of stator and rotor assemblies.
- a polymer reinforced with nano-sized particles is illustrated 50.
- a polymer composite 50 comprises a polymer host material, formed of polymer chains 52, and reinforced with a plurality of nano-sized particles 54 functionalized with chemical agents that serve as cross-linking agents.
- the polymer host material may be elastomers, thermosets or thermoplastics.
- the polymer host material may be an elastomer, such as nitrile, a copolymer of acrylonitrile and butadiene (NBR), or carboxylated acrylonitrile butadiene (XNBR), or hydrogenated acrylonitrile butadiene (HNBR), commonly referred to as highly-saturated nitrile (HSN), or carboxylated hydrogenated acrylonitrile butadiene (XHNBR), or hydrogenated carboxylated acrylonitrile butadiene (HXNBR).
- NBR acrylonitrile and butadiene
- XNBR carboxylated acrylonitrile butadiene
- HNBR hydrogenated acrylonitrile butadiene
- the polymer host material may be a flurocarbon (FKM), such as tetrafluoroethylene and propylene (FEPM), or perfluoroelastomer (FFKM).
- FKM flurocarbon
- FEPM tetrafluoroethylene and propylene
- FFKM perfluoroelastomer
- the polymer host material may also be polychloroprene rubber (CR), natural rubber (NR), polyether eurethane (EU), styrene butadiene rubber (SBR); ethylene propylene (EPR), ethylene propylene diene (EPDM) or similar elastomers.
- the polymer host material may be a thermoplastic (TPE), such as polyphenylene sulfide (PPS), polyetherketone-ketone (PEKK), polyetheretherketone (PEEK), polyetherketone (PEK), polytetrafluorethylene (PTFE), or polysulphone (PSU).
- Nano structures may include shapes, such as plates, spheres, cylinders, tubes, fibers, three- dimensional structures, linear molecules, molecular rings, branched molecules and crystalline, amorphous, and symmetric shapes.
- Nano particles may be from a variety of materials, such as carbon, silica, metals, graphite, diamond, ceramics, metal oxides, other oxides, calcium, calcium carbonate, inorganic clays, minerals, and polymer materials.
- the nano structures may be formed from silicon material, such as polysilane resins, polycarbosilane resins (PCS), polysilsesquioxane resins (POS) and polyhedral oligomeric silsesquioxane resins (POSS).
- Nano clay may be derived, for example, from montmorillonite, bentonite, hectorite, attapulgite, kaolin, mica and illite.
- Nano tubes can be formed from a variety of materials, for example, carbon. Carbon nano tubes exhibit desirable combinations of mechanical, thermal and electrical properties for applications defined by the present invention.
- Nano fibers may be derived, for example, from graphite, carbon, glass, cellulose substrate and polymer materials. Carbon nano tubes are generally in the range from approximately 0.5 nanometers to approximately 100 nanometers, at the least dimension. Carbon nano fibers are generally in the range from approximately 10 nanometers to approximately 500 nanometers, at the least dimension.
- Nano clays are generally in the range from approximately 0.1 nanometers to approximately 100 nanometers, at the least dimension.
- the polymer composite 55 comprises a polymer host material, formed of polymer chains 52 and reinforced with nano-sized particles 56 comprised of nano tubes or nano fibers.
- nano tubes can be formed as single-wall nano rubes.
- nano tubes also can be formed as multi-wall nano tubes.
- nano tubes can be formed as arrays of nano tubes.
- Nano particles may include metal oxides of zinc, iron, titanium, magnesium, silicon, aluminum, cerium, zirconium and equivalents thereof, as well as mixed metal compounds, such as indium-tin and equivalents thereof.
- Nano composite material 150 forming an elastomer element of a stator and rotor assembly 25 of the present invention is depicted.
- Nano composite material 150 is comprised of a polymer host material 152 that may include a plurality of polymers 154, 156, 158 and a plurality of nano structures. 160.
- the polymer host material 152 exhibits microporocity as represented by a plurality of regions of free volume 162.
- the nano particles 160 are positioned within free volume region 162.
- nano structure 150 may be formed from polysilane resins (PS), as depicted in Figure 10, polycarbosilane resins (PCS), as depicted in Figure 1 1, polysilsesquioxane resins (PSS), as depicted in Figure 12, or polyhedral oligomeric silsesquioxane resins (POSS), as depicted in Figure 13, as well as monomers, polymers and copolymers thereof, hi the formulas presented in FIGS.
- PS polysilane resins
- PCS polycarbosilane resins
- PSS polysilsesquioxane resins
- PES polyhedral oligomeric silsesquioxane resins
- R represents a hydrogen or an alkane, alkenyl or alkynl hydrocarbons, cyclic or linear, with 128 carbon atoms, substituted hydrocarbons R-X, aromatics where X represents halogen, phosphorus or nitrogen-containing groups.
- halogen or other inorganic groups such as phosphates and amines
- halogen group may afford additional improvements to the mechanical properties of the material.
- the incorporation of halogen group may afford additional heat resistance to the material.
- These nano structures may also include termination points, such as chain ends that contain reactive or nonreactive functionalities, such as silanols, esters, alcohols, amines or R groups.
- the polymer host material 152 and the nano structures 160 may interact via interfacial interactions, such as co-polymerization, crystallization, van der Waals interactions, covalent bonds as depicted in figure 14, ionic bonds, and cross-linking interactions between nano structure 160 and polymers 154, 156, 158 to improve the physical and chemical characteristics of the polymer thereby resulting in an extended life for the stator and rotor assembly 25 of the present invention.
- interfacial interactions such as co-polymerization, crystallization, van der Waals interactions, covalent bonds as depicted in figure 14, ionic bonds, and cross-linking interactions between nano structure 160 and polymers 154, 156, 158 to improve the physical and chemical characteristics of the polymer thereby resulting in an extended life for the stator and rotor assembly 25 of the present invention.
- the nano particle structures maybe functionalized to enhance the effective surface area and improve the availability of potential chemical reactions or catalysis sites for chemical functional groups on the nano structure.
- Surface functionalization introduces chemical functional groups to a surface, such as the surface of the polymer, thereby providing a surface layer with increased surface area and containing uniform pores with a high effective surface area, thus increasing the number of potential chemical reactions or catalysis sites on the nano particle structure.
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Abstract
Description
Claims
Priority Applications (3)
Application Number | Priority Date | Filing Date | Title |
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MX2010006839A MX2010006839A (en) | 2007-12-18 | 2008-12-11 | Nano particle reinforced polymer element for a stator and rotor assembly. |
AU2008343949A AU2008343949A1 (en) | 2007-12-18 | 2008-12-11 | Nano particle reinforced polymer element for a stator and rotor assembly |
EP08866443A EP2252768A2 (en) | 2007-12-18 | 2008-12-11 | Nano particle reinforced polymer element for a stator and rotor assembly |
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US12/002,710 US20090152009A1 (en) | 2007-12-18 | 2007-12-18 | Nano particle reinforced polymer element for stator and rotor assembly |
US12/002,710 | 2007-12-18 |
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WO2009085112A2 true WO2009085112A2 (en) | 2009-07-09 |
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US (1) | US20090152009A1 (en) |
EP (1) | EP2252768A2 (en) |
AU (1) | AU2008343949A1 (en) |
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WO (1) | WO2009085112A2 (en) |
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Also Published As
Publication number | Publication date |
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AU2008343949A1 (en) | 2009-07-09 |
US20090152009A1 (en) | 2009-06-18 |
WO2009085112A3 (en) | 2009-08-27 |
EP2252768A2 (en) | 2010-11-24 |
MX2010006839A (en) | 2010-08-11 |
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