Non-metallic compliant sand control screen

Information

  • Patent Grant
  • 11927082
  • Patent Number
    11,927,082
  • Date Filed
    Monday, February 17, 2020
    4 years ago
  • Date Issued
    Tuesday, March 12, 2024
    2 months ago
Abstract
A sand screen apparatus for use in a downhole operation for hydrocarbon recovery includes a non-metallic material and a mechanical retainer. The non-metallic material has a compressed state and an expanded state, and includes a base polymer, and one or a plurality of smart fillers dispersed with a polymeric matrix of the non-metallic material. The mechanical retainer compresses the non-metallic material in the compressed state. The one or the plurality of smart fillers react with the base polymer in the expanded state after exposure to a wellbore condition.
Description
BACKGROUND

In many hydrocarbon wells, inflowing fluid passes through a sand screen which filters out particulates from the inflowing oil or gas. The sand screen prevents sand from entering the wellbore and reduces damage that may occur by erosion. Conventionally, sand screens are made with a metallic mesh material. Once the sand screen is placed into the wellbore, gravel packs are pumped to fill the annulus between the screen and the formation.


In other instances, some metallic sand screens are expandable and are expanded downhole after placement in the wellbore. The result is a reduction in the annulus between the screen and the formation. The expandable screens in many instances have a limited expansion ratio and the ability of the expandable screen to conform to borehole irregularities may not be satisfactory. Further, the ability of the expandable sand screen to resist borehole collapse may be reduced. Conventional sand screens are rated to resist greater external pressure than expandable sand screens. Expandable sand screens resist less external pressure because of plastic deformation experienced by their metallic components.


Recently, self-conformable polymer screens have been developed by using thermoplastic urethane (TPU) and implementing a shape memory concept. The polymeric screen has an open cell structure, which has been compressed. The polymeric screen is then placed into a wellbore and expanded by controlling the glass transition temperature of the polymeric material by utilizing an activation fluid, such as acetyl acetone, for example. The activation fluid is difficult to handle at the well site because the flash point of the activation fluid is relatively low, and a special formulation of the fluid is required. Once in the borehole, the polymeric TPU foam material softens and tries to return to its original expanded shape. The expansion outer diameter was designed to be higher than the borehole internal diameter, resulting in the TPU foam conforming to the entire length of an even irregularly shaped, e.g., open hole, borehole, which can circumvent the need to pump gravel slurry in a gravel packing operation. However, one of the disadvantages of the foam material used in these sand screens is the weak mechanical properties of these foams when expanded. The application is limited by the pressure and temperature rating. If an expanded foam fails during a downhole operation, well control may be lost. Further, screen collapse under wellbore pressure may lead to a loss of permeability and a stuck completion string in the wellbore, which may be difficult to repair or change.


SUMMARY

In one or more embodiments of the present disclosure, a sand screen apparatus for use in a downhole operation for hydrocarbon recovery includes a non-metallic material having a compressed state and an expanded state, the non-metallic material including a base polymer, and one or a plurality of smart fillers dispersed within a polymeric matrix of the non-metallic material, and a mechanical retainer that compresses the non-metallic material in the compressed state. In one or more embodiments of the present disclosure, the one or the plurality of smart fillers react with the base polymer in the expanded state after exposure to a wellbore condition.


A well completion method according to one or more embodiments of the present disclosure includes covering at least one base pipe with a non-metallic material comprising a base polymer and one or a plurality of smart fillers, compressing the non-metallic material with a mechanical retainer, running the base pipe to a location in a wellbore, expanding the non-metallic material, conforming the non-metallic material to a wall of the wellbore, stiffening the non-metallic material, filtering fluids through the non-metallic material to the base pipe, detaching the non-metallic material from the base pipe, and lifting the base pipe out of the wellbore.


A method of completing a wellbore in a subterranean formation according to one or more embodiments of the present disclosure includes positioning an expandable sand control apparatus in the wellbore and forming an annulus between the sand control apparatus and the wellbore, the sand control apparatus having a cellular open cell structure with a non-metallic material including a base polymer, and one or a plurality of smart fillers, the non-metallic material configured to expand and fill the annulus.


However, many modifications are possible without materially departing from the teachings of this disclosure. Accordingly, such modifications are intended to be included within the scope of this disclosure as defined in the claims.





BRIEF DESCRIPTION OF THE DRAWINGS

Certain embodiments of the disclosure will hereafter be described with reference to the accompanying drawings, wherein like reference numerals denote like elements. It should be understood, however, that the accompanying figures illustrate the various implementations described herein and are not meant to limit the scope of various technologies described herein, and:



FIG. 1 is a sectional view of a sand screen positioned in a wellbore according to one or more embodiments of the present disclosure;



FIGS. 2(A) and 2(B) show further details of the sand screen according to one or more embodiments of the present disclosure;



FIG. 3 shows a schematic drawing of a chemical foaming process according to one or more embodiments of the present disclosure;



FIG. 4 shows an example of an open cell foam according to one or more embodiments of the present disclosure;



FIG. 5 shows an example of superabsorbent polymers according to one or more embodiments of the present disclosure;



FIGS. 6(A) and 6(B) provide an example of elastomer foam morphology before and after brine swell;



FIGS. 7(A) and 7(B) show an example of mechanical compress and release according to one or more embodiments of the present disclosure;



FIG. 7(C) shows a photograph of different degradable layers, which may be used as a mechanical retainer, according to one or more embodiments of the present disclosure;



FIG. 7(D) shows a photograph of different degradable layers after 48 hrs in KCl 3% brine at different temperatures;



FIG. 7(E) shows tensile properties of a degradable layer (mechanical retainer) after 48 hrs in KCl 3% brine at 200° F. according to one or more embodiments of the present disclosure;



FIG. 8 shows an example of how a mechanical retainer (i.e., degradable layer or film) may be used according to one or more embodiments of the present disclosure.



FIG. 9 shows an example of TPU chemical structures according to one or more embodiments of the present disclosure;



FIG. 10 shows an example of a chemical structure of an ether-ester thermoplastic elastomer according to one or more embodiments of the present disclosure;



FIG. 11 shows a schematic drawing of a polyamide-polyether thermoplastic elastomer structure according to one or more embodiments of the present disclosure;



FIG. 12 shows an example of a cross-linked polyethylene (XLPE) foam according to one or more embodiments of the present disclosure;



FIGS. 13(A) and 13(B) show a polyolefin foam morphology at 200 μm resolution and 100 μm resolution, respectively;



FIG. 14 shows an example of a silicone foam process according to one or more embodiments of the present disclosure;



FIG. 15 shows an example of a silicone foam according to one or more embodiments of the present disclosure;



FIG. 16 shows an example of an epoxy foam according to one or more embodiments of the present disclosure;



FIGS. 17(A) and 17(B) show an epoxy foam morphology at 500 μm resolution and 200 μm resolution, respectively; and



FIG. 18 is an example of a polyimide open cell foam according to one or more embodiments of the present disclosure.





DETAILED DESCRIPTION

In the following description, numerous details are set forth to provide an understanding of some embodiments of the present disclosure. However, it will be understood by those of ordinary skill in the art that the system and/or methodology may be practiced without these details and that numerous variations or modifications from the described embodiments may be possible.


In the specification and appended claims: the terms “up” and “down,” “upper” and “lower,” “upwardly” and “downwardly,” “upstream” and “downstream,” “uphole” and “downhole,” “above” and “below,” and other like terms indicating relative positions above or below a given point or element are used in this description to more clearly describe some embodiments of the disclosure.


The present disclosure generally relates to using a non-metallic material with smart fillers for sand control applications. Using smart fillers allows the non-metallic materials to self-expand to conform to the irregular shape of the wellbore. The non-metallic materials are easy to manufacture by compounding and injection molding. Without the need for additional activation fluids, the non-metallic materials according to one or more embodiments of the present disclosure are much safer over conventional TPU materials. The non-metallic materials according to one or more embodiments of the present disclosure also provide excellent thermal stability allowing them to be used at much higher temperatures, up to 150° C. for example, for long-term applications. In contrast, conventional TPU materials are only operable up to 85° C.


Referring now to FIG. 1, a sectional view of a sand screen positioned in a wellbore according to one or more embodiments of the present disclosure is shown. Specifically, the wellbore 100 includes an open bore hole 102, a production tubing string 104, which may be a base pipe according to one or more embodiments, and a sand screen 106. While wellbore 100 is illustrated as being a substantially vertical, uncased well, it should be recognized that the subject disclosure is equally applicable for use in cased wellbores as well as in horizontal and/or inclined wellbores. The sand screen 106 includes a filter member 108 and a compliant material 112. The sand screen 106 is shown positioned in the wellbore 100 adjacent a producing formation 114. According to one or more embodiments of the present disclosure, the compliant material 112 may be the only filtration agent without the use of any filter member 108. The compliant material 112 may be a porous material and therefore acts as a filtration agent. In one or more embodiments, the filter member 108 can be configured for structural support of the compliant material 112.


If it becomes necessary to remove the tubing 104 and the filter member 108 for some reason, (e.g., work over the well to restore production), the tubing 104 and the filter member 108 may be pulled out of the wellbore 100. The compliant material 112 may be attached to the filter member 108 or the tubing 104 via an attachment 110. In some embodiments, the attachment 110 may include a material that may degrade with exposure to downhole temperatures, fluids or time, e.g., a glue, or a degradable layer or film. In other embodiments, the compliant material 112 may be attached to the filter member 108 or the tubing 104 with an attachment 110 that is time-invariant. In a non-limiting example, this may involve shear screws, which would shear at a given force and release the attachment 110. Degradation of the material may be important in situations when the run-in forces are greater than that available during fishing. If the run-in forces are less than that available during fishing, degradation is not necessary. In certain situations where the compliant material 112 is not detached from the filter member 108 or from the tubing 104, there may be multiple “flexible screens” comprising the compliant material, which results in the axial pull being divided. In these situations, a provision is made for a weak plane below each “flexible screen” so that the tubing below each “flexible screen” is parted, and each “flexible screen” may be removed sequentially.


Still referring to FIG. 1, in a well completion method according to one or more embodiments of the present disclosure, at least one base pipe 104 may be covered with a compliant material 112, which may be a non-metallic compliant material that includes a base polymer and one or more smart fillers, as further described below. The compliant material 112 covering the base pipe 104 may be compressed with a mechanical retainer before running the base pipe 104 to a location in the wellbore 100, as further described below. Upon exposure to a condition in the wellbore 100, the compliant material 112 covering the base pipe 104 may expand due to reaction of the one or more smart fillers, and release or degradation of the mechanical retainer, as further described below. In one or more embodiments, the smart fillers stiffen the compliant material 112 during expansion. As the compliant material 112 expands into and fills the annulus, the compliant material 112 conforms to a wall of the wellbore 100. Because the compliant material 112 is able to conform to the wellbore 100 wall in this way, the compliant material 112 is able to filter debris including sand from fluids from the producing formation 114 to the base pipe 104. After the downhole operation is complete, the compliant material 112 may be detached from the base pipe 104, and the base pipe 104 may be lifted out of the wellbore 100.



FIGS. 2(A) and 2(B) show further details of the non-metallic compliant screen, according to one or more embodiments of the present disclosure. FIGS. 2(A) and 2(B) show a compliant screen 211, which comprises a non-metallic compliant material 209 and a filter material or screen 207, which may be constructed in a variety of configurations, e.g., a slotted liner. FIG. 2(A) shows the compliant screen 211 in its initial, unexpanded state, and FIG. 2(B) shows the compliant screen 211 in its expanded state. The compliant screen 211 is initially compliant, and according to one or more embodiments, the non-metallic compliant material 209 of the compliant screen 211 includes a base polymer and one or more smart fillers that facilitate swelling and/or reinforcement of the non-metallic compliant material 209 upon reaction with the base polymer.


Referring now to FIG. 3, a schematic drawing of a chemical foaming process using a structural foam molding machine is shown, in accordance with one or more embodiments of the present disclosure. In the foaming process according to one or more embodiments of the present disclosure, a polymer open cell structure can be manufactured by utilizing various chemical foaming agents during a molding process. Polymer materials according to one or more embodiments of the present disclosure may be prepared by being compounded with smart fillers, which may include swellable or reinforcing fillers, and/or foaming agents. In this way, the polymer materials can be manufactured with a chemical foaming agent to create open cell structures, such as the open cell foam shown in FIG. 4, for example. Using this chemical foaming process, the non-metallic compliant material according to one or more embodiments of the present disclosure may assume a foam structure, which may be a microfoam structure. Advantageously, the foam structure can allow production fluid to pass through, while blocking solid debris from the wellbore, such as sands.


Chemical foaming agents are chemical substances that decompose during heating, and the resulting gaseous decomposition products are dispersed through polymer melts. To obtain a uniform cell structure, the gas is either injected or evolved by heat and must be thoroughly dispersed in the polymer melts. Some of the essential factors influencing this process are the particle size of the foaming agent, the dispersive properties of the machine, the decomposition rate of the foaming agent, and the melt viscosity of the thermoplastic resin being processed. In one or more embodiments of the present disclosure, CO2, N2, and hydrofluorocarbons (HFCs) may be used as the chemical foaming agents, for example.


As previously described, the non-metallic compliant material for the compliant screen may include a base polymer and one or more smart fillers. According to one or more embodiments of the present disclosure, the base polymer may include at least one of polyurethane, thermoplastic polyurethane, thermoplastic elastomer, poly ether-ester block copolymer, polyamide polyether thermoplastic elastomer, polyolefin, cross-linked polyethylene, silicone rubber, nitrile butadiene rubber (NBR), hydrogenated nitrile butadiene rubber (HNBR), ethylene propylene diene monomer rubber (EPDM), any type of fluoroelastomer, epoxy, and polyimide, for example.


Also, according to one or more embodiments of the present disclosure, the one or more smart fillers may include at least one of a swellable filler and/or a reinforcing filler. For example, the smart fillers may include at least one swellable filler such as superabsorbent polymers (SAP), ethylene propylene diene monomer rubber (EPDM), and hydrogenated nitrile butadiene rubber (HNBR), and/or at least one reinforcing filler such as Portland cement, aluminous cement, fly ash, slag cement, MgO, ZnO, Ca(OH)2, ZnCl2, MgCl2, CaCl2, CaCO3, Na2CO3, and K2CO3.


Regarding swellable smart fillers, this filler/polymer can increase in volume when deployed into well fluid or brine. SAP, as shown in FIG. 5 for example, is a type of hydrophilic polymer (cross-linked hydrogel) having water-absorbing capacity from 100 g/g up to 2000 g/g, in which the absorbed water is scarcely removable even under pressure because the water molecules are held tightly in the network by hydrogen bonding. Using a cross-linked polymer like SAP will facilitate the passage of water through the three-dimensional network of the structure, while retaining the polymer structure, which can force the structure to swell.


The SAPs that may be used in accordance with one or more embodiments of the present disclosure include cross-linked forms of polyacrylate (acrylic acid and acrylamide), polyvinyl alcohol, poly(ethylene oxide), starch-acrylate copolymer, carboxymethyl cellulose, and other hydrophilic swellable polymers. As understood by those having skill in the art, the degree of swelling and the swelling rate of SAPs depend on the type of cross-linked polymer, the conditions of the water with respect to pH, salinity, temperature, and pressure, the duration of immersion in a solution, and the design of the samples.


Referring now to FIGS. 6(A) and 6(B), an example of elastomer foam morphology before and after brine swell is provided. In the example shown in FIGS. 6(A) and 6(B), the elastomer foam includes smart fillers, such as those previously described, to facilitate swelling in brine. The elastomer foam itself may also swell in the presence of brine, independent of any swelling contributed by the smart fillers. As shown in FIGS. 6(A) and 6(B), the morphology of the elastomer foam is relatively constant before and after swelling in brine. Such consistent morphology before and after swelling suggests that the elastomer foam is a viable filter medium with advantageous permeability properties.


In addition to smart fillers, the non-metallic compliant material for the compliant screen may also include other “non-smart” fillers such as talc, mica, silica, carbon black, nanographene, carbon nanotubes, glass fibers, and carbon fillers for additional support.


The fillers according to one or more embodiments of the present disclosure may be surface treated to improve the bonding with the polymeric matrix of the non-metallic compliant material. Self-reinforcing fillers such as cement may react with completion brine or water to improve strength of the non-metallic compliant material.


According to one or more embodiments of the present disclosure, the screen may include a mechanical retainer that compresses the non-metallic compliant material in a compressed state. When the non-metallic compliant material is deployed downhole in the compressed state due to compression by the mechanical retainer, a wellbore condition downhole such as a temperature change or a lapse in time, for example, may cause the mechanical retainer to release from the non-metallic compliant material. Release of the mechanical retainer will allow the non-metallic compliant material to transition from the compressed state to an expanded state. In the expanded state, the non-metallic compliant material can expand to a larger shape as the smart fillers dispersed within a polymer matrix of the non-metallic compliant material react with downhole fluids to increase in size. In one or more embodiments, the mechanical retainer may be a degradable polymeric wrapping tape that dissolves in water or other downhole fluids when exposed to the wellbore condition. The mechanical retainer may also be thermally molded to the non-metallic compliant material.


Referring now to FIGS. 7(A) and 7(B), an example of mechanical compress and release according to one or more embodiments of the present disclosure is shown. As shown, the polymer foam or non-metallic compliant material is thermally molded and/or mechanically wrapped by degradable polymers, which compresses the polymer foam. After exposure to a wellbore condition, the degradable polymers may degrade or otherwise release from the polymer foam or non-metallic compliant material, allowing the polymer foam or non-metallic compliant material to transition from the compressed state to the expanded state. In the expanded state, the smart fillers, which may include swellable fillers and/or reinforcing fillers, react with the base polymer of the polymer foam or non-metallic compliant material. In this way, the non-metallic compliant material can expand to a larger shape as the smart fillers dispersed within the polymer matrix of the non-metallic compliant material react with downhole fluids to increase in size. In addition, the smart fillers may also increase the stiffness of the polymer matrix, thereby strengthening the non-metallic compliant material to better withstand downhole pressures. Moreover, the non-metallic compliant material can expand to conform to an irregular shape of the wellbore, as shown in FIG. 2(B) as previously described, for example. Due to the smart fillers, the non-metallic compliant material experiences improved and sustained strength while in the expanded state. The non-metallic compliant material also experiences a modulus increase from the compressed state to the expanded state. In view of the above disclosure, FIGS. 7(A) and 7(B) show the progression of the polymer foam or non-metallic compliant material from the compressed state to the expanded state according to one or more embodiments of the present disclosure.


Referring now to FIG. 7(C), a photograph of different degradable layers, which may be used as a mechanical retainer, according to one or more embodiments of the present disclosure is shown. As shown, the degradable layers may be sufficiently thin to resemble and behave like a degradable film. FIG. 7(D) shows a photograph of different degradable layers after 48 hrs in KCl 3% brine at different temperatures. As shown in FIG. 7(D), the degradation rate of the different degradable layers increases with increased temperature. As such, the degradation rate of the degradable layers according to one or more embodiments of the present disclosure may be controlled via temperature. Referring now to FIG. 7(E), the tensile properties of a degradable layer (mechanical retainer) after 48 hrs in KCl 3% brine at 200° F. according to one or more embodiments of the present disclosure is shown. As shown, the degradable layer, which may be a mechanical retainer according to one or more embodiments of the present disclosure, degrades, dissolves, and otherwise exhibits low mechanical properties (i.e., about 200 psi tensile stress and about 20% to 25% elongation after 48 hrs in KCl 3% brine at 200° F.) as compared against the controls, which show about 1200 psi tensile stress and exhibit an elongation percentage in a range of 300% to 400%. Indeed, as shown, the degradable layer according to one or more embodiments of the present disclosure exhibits excellent degradability as compared against the controls.


Referring now to FIG. 8, an example of how a mechanical retainer may be used according to one or more embodiments of the present disclosure is shown. By using a chemical foaming process such as that described with respect to FIG. 3, for example, polymeric materials may be transformed into cellular structures. These cellular structure materials may be compressed into a smaller cylinder shape by using a mechanical degradable polymer tape wrapping process, as shown in FIG. 8, for example. As shown in FIG. 8, the mechanical retainer 802, which may be a degradable polymeric wrapping tape as previously described, may be mechanically wrapped around the cellular structures or non-metallic compliant material 209, thereby compressing the non-metallic compliant material 209 before deployment in the wellbore. In one or more embodiments, commercially available water-soluble tape may be used for the mechanical retainer 802, for example.


Various examples of the non-metallic compliant material according to one or more embodiments of the present disclosure will now be described. FIG. 9 provides examples of thermoplastic urethane (TPU) chemical structures according to one or more embodiments of the present disclosure. For example, in the previously described chemical foaming process with reference to FIG. 3, a polymer foam may be manufactured using TPU (such as one of the chemical structures shown in FIG. 9) compounded with smart fillers, which may include swellable or reinforcing fillers for the polymer material, and a chemical foaming agent as previously described. The resulting TPU polymer foam may be an open cell foam, and may be used as the non-metallic compliant material for the sand screen apparatus according to one or more embodiments of the present disclosure.



FIG. 10 provides another example of a chemical structure of a base polymer that may be used in the non-metallic compliant material according to one or more embodiments of the present disclosure. Specifically, FIG. 10 shows a block copolymer of a thermoplastic polyester elastomer (TPE). For example, in the previously described chemical foaming process with reference to FIG. 3, a polymer foam may be manufactured using TPE (such as the block copolymer shown in FIG. 10) compounded with smart fillers, which may include swellable or reinforcing fillers for the polymer material, and a chemical foaming agent as previously described. The resulting TPE polymer foam may be used as the non-metallic compliant material for the sand screen apparatus according to one or more embodiments of the present disclosure, which may be mechanically compressed using degradable polymers before deployment downhole as previously described. In a downhole operation, mechanical release of the degradable polymers and reaction of the smart fillers with the TPE base polymer facilitate expansion of the non-metallic compliant material in accordance with one or more embodiments of the present disclosure, as previously described. According to one or more embodiments of the present disclosure, commercially available Hytrel® may be used as the TPE base polymer of the non-metallic compliant material.



FIG. 11 provides another example of a chemical structure of a base polymer that may be used in the non-metallic compliant material according to one or more embodiments of the present disclosure. Specifically, FIG. 11 shows a polyamide-polyether (PA-PE) thermoplastic elastomer as the chemical structure. For example, in the previously described chemical foaming process with reference to FIG. 3, a polymer foam may be manufactured using TPE, PA-PE (such as the polymers shown in FIG. 11) compounded with smart fillers, which may include swellable or reinforcing fillers for the polymer material, and a chemical foaming agent as previously described. The resulting TPE, PA-PE polymer foam may be used as the non-metallic compliant material for the sand screen apparatus according to one or more embodiments of the present disclosure, which may be mechanically compressed using degradable polymers before deployment downhole as previously described. In a downhole operation, mechanical release of the degradable polymers and reaction of the smart fillers with the TPE, PA-PE base polymer facilitate expansion of the non-metallic compliant material in accordance with one or more embodiments of the present disclosure, as previously described.



FIG. 12 provides another example of a base polymer that may be used in the non-metallic compliant material according to one or more embodiments of the present disclosure. For example, FIG. 12 shows an example of a polyolefin, which may be a cross-linked polyethylene (XLPE) foam, according to one or more embodiments of the present disclosure. Advantageously, cross-linking polyethylene can significantly improve the low-temperature impact strength, the abrasion resistance, and the environmental stress cracking resistance of the chemical structure. However, cross-linking polyethylene may reduce the hardness and rigidity of the chemical structure to a degree. Because XLPE is similar to elastomers, XLPE does not melt and is thermally resistant. Further, the maximum shear modulus of the chemical structure increases with increasing cross-linking density (even at higher temperatures). Indeed, XLPE has significantly enhanced properties compared to ordinary polyethylene. For example, the cross-linking in XLPE enhances the temperature properties in the base polymer. Adequate strength to 120-150° C. is maintained, and chemical stability is enhanced by resisting dissolution. Low-temperature properties are improved. Impact and tensile strength, scratch resistance, and resistance to brittle fracture are enhanced.


According to one or more embodiments of the present disclosure, the XLPE foam shown in FIG. 12 may be an open cell foam, which may be manufactured by using various chemical foaming agents during a molding process, as previously described. For example, in the previously described chemical foaming process with reference to FIG. 3, an open cell foam may be manufactured using XLPE compounded with smart fillers, which may include swellable or reinforcing fillers for the polymer material, and a chemical foaming agent as previously described. The resulting XLPE open cell foam may be used as the non-metallic compliant material for the sand screen apparatus according to one or more embodiments of the present disclosure, which may be mechanically compressed using degradable polymers before deployment downhole as previously described. For example, FIGS. 13(A) and 13(B) show a polyolefin foam morphology at 200 μm resolution and 100 μm resolution, respectively. As shown in FIGS. 13(A) and 13(B), the polyolefin foam morphology includes an open cell structure. In a downhole operation, mechanical release of the degradable polymers and reaction of the smart fillers with the XLPE base polymer facilitate expansion of the non-metallic compliant material in accordance with one or more embodiments of the present disclosure, as previously described.



FIGS. 14 and 15 provide another example of a base polymer that may be used in the non-metallic compliant material according to one or more embodiments of the present disclosure. For example, FIG. 14 shows an example of a silicone foam process, and FIG. 15 shows examples of silicone foam. As shown in FIG. 14, mixing the constituent components of silicone foam together causes hydrogen gas to form. The hydrogen gas causes the material to expand into a foam. In one or more embodiments, the foam may be cured to improve its strength and ease of handling.


According to one or more embodiments of the present disclosure, the silicone foam shown in FIGS. 14 and 15 may be an open cell foam, which may be manufactured by using various chemical foaming agents during a molding process, as previously described. For example, in the previously described chemical foaming process with reference to FIG. 3, an open cell foam may be manufactured using silicone foam compounded with smart fillers, which may include swellable or reinforcing fillers for the polymer material, and a chemical foaming agent as previously described. The resulting silicone open cell foam may be used as the non-metallic compliant material for the sand screen apparatus according to one or more embodiments of the present disclosure, which may be mechanically compressed using degradable polymers before deployment downhole as previously described. In a downhole operation, mechanical release of the degradable polymers and reaction of the smart fillers with the silicone foam base polymer facilitate expansion of the non-metallic compliant material in accordance with one or more embodiments of the present disclosure, as previously described.



FIG. 16 provides another example of a base polymer that may be used in a non-metallic compliant material according to one or more embodiments of the present disclosure. For example, FIG. 16 shows an example of an epoxy foam. According to one or more embodiments of the present disclosure, the epoxy foam shown in FIG. 16 may be an open cell foam, which may be manufactured by using various chemical foaming agents during a molding process, as previously described. For example, in the previously described chemical foaming process with reference to FIG. 3, an open cell foam may be manufactured using epoxy foam compounded with smart fillers, which may include swellable or reinforcing fillers for the polymer material, and a chemical foaming agent as previously described. FIGS. 17(A) and 17(B) show an epoxy foam morphology at 500 μm resolution and 200 μm resolution, respectively. As shown in FIGS. 17(A) and 17(B), the epoxy foam morphology includes an open cell structure. The resulting epoxy open cell foam may be used as the non-metallic compliant material for the sand screen apparatus according to one or more embodiments of the present disclosure, which may be mechanically compressed using degradable polymers before deployment downhole as previously described. In a downhole operation, mechanical release of the degradable polymers and reaction of the smart fillers with the epoxy foam base polymer facilitate expansion of the non-metallic compliant material in accordance with one or more embodiments of the present disclosure, as previously described.



FIG. 18 provides another example of a base polymer that may be used in a non-metallic compliant material according to one or more embodiments of the present disclosure. For example, FIG. 18 shows an example of a polyimide open cell foam. According to one or more embodiments of the present disclosure, the polyimide open cell foam shown in FIG. 18 may be manufactured by using various chemical foaming agents during a molding process, as previously described. For example, in the previously described chemical foaming process with reference to FIG. 3, an open cell foam may be manufactured using polyimide compounded with (or without) smart fillers, which may include swellable or reinforcing fillers for the polymer material, and a chemical foaming agent as previously described. The resulting polyimide open cell foam may be used as the non-metallic compliant material for the sand screen apparatus according to one or more embodiments the present disclosure, which may be mechanically compressed using degradable polymers before deployment downhole as previously described. In a downhole operation, mechanical release of the degradable polymers and reaction of the smart fillers with the polyimide base polymer facilitate expansion of the non-metallic compliant material in accordance with one or more embodiments of the present disclosure, as previously described.


The polyimide open cell foam of FIG. 18, which may be used as the non-metallic compliant material for the sand screen apparatus according to one or more embodiments the present disclosure, can withstand high temperature applications up to 300° C. Further, the polyimide open cell foam is flexible and recovers sufficiently after mechanical compression by the degradable polymers has been released. Moreover, the formulation of the polyimide open cell foam may be customized with smart fillers in order to enhance compliance and reinforcement.


Although a few embodiments of the disclosure have been described in detail above, those of ordinary skill in the art will readily appreciate that many modifications are possible without materially departing from the teachings of this disclosure. Accordingly, such modifications are intended to be included within the scope of this disclosure as defined in the claims.

Claims
  • 1. A sand screen apparatus for use in a downhole operation for hydrocarbon recovery, comprising: a non-metallic material having a compressed state and an expanded state, the non-metallic material comprising: a base polymer; anda plurality of smart fillers dispersed within a polymeric matrix of the non-metallic material, wherein a first smart filler of the plurality of smart fillers is configured to facilitate swelling of the non-metallic material in response to a wellbore condition, and wherein a second smart filler of the plurality of smart fillers is configured to facilitate stiffening of the non-metallic material in response to the wellbore condition; anda mechanical retainer that compresses the non-metallic material in the compressed state.
  • 2. The apparatus of claim 1, wherein the non-metallic material comprises a foam structure.
  • 3. The apparatus of claim 1, wherein the non-metallic material comprises an open cell foam.
  • 4. The apparatus of claim 1, wherein the mechanical retainer is a degradable polymeric wrapping tape.
  • 5. The apparatus of claim 4, wherein the wellbore condition causes the degradable polymeric wrapping tape to dissolve.
  • 6. The apparatus of claim 1, wherein the wellbore condition causes the mechanical retainer to release from the non-metallic material.
  • 7. The apparatus of claim 6, wherein the non-metallic material conforms to a wellbore in the expanded state.
  • 8. The apparatus of claim 1, wherein the base polymer comprises: polyurethane;thermoplastic polyurethane;thermoplastic elastomer;poly ether-ester block copolymer;polyamide polyether thermoplastic elastomer;polyolefin;cross-linked polyethylene;silicone rubber;nitrile butadiene rubber (NBR);hydrogenated nitrile butadiene rubber (HNBR);ethylene propylene diene monomer rubber (EPDM);fluoroelastomer;epoxy;polyimide; orany combination thereof.
  • 9. The apparatus of claim 1, wherein the one or the plurality of smart fillers comprises: superabsorbent polymer;ethylene propylene diene monomer rubber (EPDM);hydrogenated nitrile butadiene rubber (HNBR);Portland cement;aluminous cement;fly ash, slag cement;MgO;ZnO;Ca(OH)2;ZnCl2;MgCl2;CaCl2;CaCO3;Na2CO3;K2CO3; orany combination thereof.
  • 10. The apparatus of claim 1, wherein the non-metallic material experiences a modulus increase from the compressed state to the expanded state.
  • 11. The apparatus of claim 1, wherein the first smart filler is configured to undergo a first chemical reaction in response to the wellbore condition to facilitate the swelling.
  • 12. The apparatus of claim 11, wherein the second smart filler is configured to undergo a second chemical reaction in response to the wellbore condition to facilitate to the stiffening.
  • 13. The apparatus of claim 1, wherein: the base polymer comprises: polyurethane;thermoplastic polyurethane;a thermoplastic elastomer;a poly ether-ester block copolymer;a polyamide polyether thermoplastic elastomer;polyolefin;cross-linked polyethylene;silicone rubber;nitrile butadiene rubber (NBR);hydrogenated nitrile butadiene rubber (HNBR);ethylene propylene diene monomer rubber (EPDM);a fluoroelastomer;epoxy;polyimide; orany combination thereof;the first smart filler comprises: a superabsorbent polymer (SAP);ethylene propylene diene monomer rubber (EPDM);hydrogenated nitrile butadiene rubber (HNBR); orany combination thereof; andthe second smart filler comprises: Portland cement;aluminous cement;fly ash, slag cement;MgO;ZnO;Ca(OH)2;ZnCl2;MgCl2;CaCl2);CaCO3;Na2CO3;K2CO3; orany combination thereof.
  • 14. A well completion method, comprising: covering at least one base pipe with a non-metallic material, the non-metallic material comprising: a base polymer; anda plurality of smart fillers, wherein a first smart filler of the plurality of smart fillers is configured to facilitate swelling of the non-metallic material in response to a wellbore condition, and wherein a second smart filler of the plurality of smart fillers is configured to facilitate stiffening of the non-metallic material in response to the wellbore condition;compressing the non-metallic material with a mechanical retainer;running the base pipe to a location in a wellbore;expanding the non-metallic material;conforming the non-metallic material to a wall of the wellbore;stiffening the non-metallic material;filtering fluids through the non-metallic material to the base pipe;detaching the non-metallic material from the base pipe; andlifting the base pipe out of the wellbore.
  • 15. The method of claim 14, wherein the mechanical retainer is a degradable polymeric wrapping tape.
  • 16. The method of claim 15, wherein the expanding step comprises dissolving degradable polymeric wrapping tape.
  • 17. The method of claim 14, wherein the expanding step comprises releasing the mechanical retainer.
  • 18. A method of completing a wellbore in a subterranean formation, comprising: positioning an expandable sand control apparatus in the wellbore such that an annulus is formed between the expandable sand control apparatus and the wellbore, the expandable sand control apparatus comprising a non-metallic material having an open cell structure, the non-metallic material comprising: a base polymer; anda plurality of smart fillers, wherein a first smart filler of the plurality of smart fillers is configured to facilitate expansion of the non-metallic material to fill the annulus in response to a wellbore condition of the wellbore, and wherein a second smart filler of the plurality of smart fillers is configured to facilitate stiffening of the non-metallic material in response to the wellbore condition.
  • 19. The method of claim 18, further comprising compressing the expandable sand control apparatus with a mechanical retainer before the positioning step.
  • 20. The method of claim 19, wherein the mechanical retainer is a degradable polymeric wrapping tape.
CROSS-REFERENCE TO RELATED APPLICATION

This application is a National Stage Entry of International Application No. PCT/US2020/018495, filed Feb. 17, 2020, which is based on and claims priority to U.S. Provisional Patent Application No. 62/808,132, filed Feb. 20, 2019, which is incorporated by reference in its entirety.

PCT Information
Filing Document Filing Date Country Kind
PCT/US2020/018495 2/17/2020 WO
Publishing Document Publishing Date Country Kind
WO2020/172092 8/27/2020 WO A
US Referenced Citations (137)
Number Name Date Kind
2981332 Miller Apr 1961 A
2981333 Miller et al. Apr 1961 A
3099318 Miller Jul 1963 A
3712373 Bearden et al. Jan 1973 A
3816894 Howard et al. Jun 1974 A
3901320 Calderon et al. Aug 1975 A
4917183 Gaidry et al. Apr 1990 A
5310000 Arterbury et al. May 1994 A
5782299 Simone et al. Jul 1998 A
5913365 Bryant Jun 1999 A
6216788 Wilson Apr 2001 B1
6543545 Chatterji et al. Apr 2003 B1
6607032 Voll et al. Aug 2003 B2
6695054 Johnson et al. Feb 2004 B2
6766862 Chatterji et al. Jul 2004 B2
6841582 Morikawa et al. Jan 2005 B2
6935432 Nguyen Aug 2005 B2
7013979 Richard Mar 2006 B2
7048048 Nguyen et al. May 2006 B2
7168485 Johnson et al. Jan 2007 B2
7258166 Russell Aug 2007 B2
7318481 Richard Jan 2008 B2
7373991 Vaidya et al. May 2008 B2
7493947 Ross Feb 2009 B2
7581586 Russell Sep 2009 B2
7644773 Richard Jan 2010 B2
7665538 Robisson et al. Feb 2010 B2
7703520 Dusterhoft Apr 2010 B2
7743835 Willauer Jun 2010 B2
7814973 Dusterhoft et al. Oct 2010 B2
7828055 Willauer et al. Nov 2010 B2
7832490 Willauer Nov 2010 B2
7841409 Gano et al. Nov 2010 B2
7861787 Russell Jan 2011 B2
7866383 Dusterhoft et al. Jan 2011 B2
7926565 Duan et al. Apr 2011 B2
7967596 Livi Jun 2011 B2
7984760 Haeberle et al. Jul 2011 B2
8048348 Duan et al. Nov 2011 B2
8127831 Haeberle et al. Mar 2012 B2
8196653 Fripp et al. Jun 2012 B2
8245778 Yeh et al. Aug 2012 B2
8256510 Holderman et al. Sep 2012 B2
8291972 Dusterhoft et al. Oct 2012 B2
8302681 Fripp et al. Nov 2012 B2
8316952 Moen Nov 2012 B2
8365833 Carrejo et al. Feb 2013 B2
8490707 Robisson et al. Jul 2013 B2
8499827 Dusterhoft et al. Aug 2013 B2
8511361 Guest Aug 2013 B2
8517184 Carrejo et al. Aug 2013 B2
8528640 Agrawal Sep 2013 B2
8540032 Nutley et al. Sep 2013 B2
8551274 Guest Oct 2013 B2
8579025 Holderman et al. Nov 2013 B2
8651179 Vaidya et al. Feb 2014 B2
8664318 Guest et al. Mar 2014 B2
8678100 Guest et al. Mar 2014 B2
8684075 Guest et al. Apr 2014 B2
8701757 Greci Apr 2014 B2
8720590 Guest et al. May 2014 B2
8721958 Guest May 2014 B2
8783349 Robisson et al. Jul 2014 B2
8850706 Bonner et al. Oct 2014 B2
8875784 Kuo et al. Nov 2014 B2
8876944 Ren et al. Nov 2014 B2
8939222 Ren et al. Jan 2015 B2
8980799 Agrawal et al. Mar 2015 B2
9044914 Guest et al. Jun 2015 B2
9051805 Johnson et al. Jun 2015 B2
9068437 Carrejo et al. Jun 2015 B2
9090012 Mazyar et al. Jul 2015 B2
9155983 Guest et al. Oct 2015 B2
9174151 Lopez et al. Nov 2015 B2
9212541 Richard et al. Dec 2015 B2
9243473 Yang et al. Jan 2016 B2
9322249 Fripp et al. Apr 2016 B2
9388671 Holderman Jul 2016 B2
9399902 Greci Jul 2016 B2
9434026 Koli et al. Sep 2016 B2
9441458 Carrejo et al. Sep 2016 B2
9441462 Chakraborty et al. Sep 2016 B2
9725988 Gano et al. Aug 2017 B2
9777548 Prieto et al. Oct 2017 B2
9878486 Liu et al. Jan 2018 B2
10072482 Hodge et al. Sep 2018 B2
10107093 Yeh et al. Oct 2018 B2
10184323 Kim et al. Jan 2019 B2
10435554 Yun et al. Oct 2019 B2
10443339 Yun et al. Oct 2019 B2
10450844 Kim et al. Oct 2019 B2
10487630 Davis et al. Nov 2019 B2
10508185 Murugesan et al. Dec 2019 B2
10577896 Dowsett et al. Mar 2020 B2
10767449 Lazo et al. Sep 2020 B2
10781672 Lazo et al. Sep 2020 B2
10781673 Kim et al. Sep 2020 B2
10781674 Bourgneuf et al. Sep 2020 B2
11060382 Sherman Jul 2021 B2
20030089495 Bixenman May 2003 A1
20040261994 Nguyen et al. Dec 2004 A1
20050034860 Lauritzen Feb 2005 A1
20050056425 Grigsby et al. Mar 2005 A1
20060175065 Ross Aug 2006 A1
20060185849 Edwards et al. Aug 2006 A1
20070012444 Horgan et al. Jan 2007 A1
20080035330 Richards Feb 2008 A1
20080083493 Ridges et al. Apr 2008 A1
20080217002 Simonds et al. Sep 2008 A1
20080264647 Li Oct 2008 A1
20090151942 Bernardi, Jr. Jun 2009 A1
20090173497 Dusterhoft Jul 2009 A1
20100069469 Young et al. Mar 2010 A1
20100252254 Nutley et al. Oct 2010 A1
20100258302 Bonner et al. Oct 2010 A1
20110086942 Robisson et al. Apr 2011 A1
20110098202 James et al. Apr 2011 A1
20110232901 Carrejo et al. Sep 2011 A1
20110247813 Moen Oct 2011 A1
20110303411 Todd et al. Dec 2011 A1
20120017134 Lee et al. Jan 2012 A1
20120211226 Guest et al. Aug 2012 A1
20130032969 Guest et al. Feb 2013 A1
20130092394 Holderman et al. Apr 2013 A1
20130161026 Garza et al. Jun 2013 A1
20140020910 Falkner et al. Jan 2014 A1
20140332220 Garza et al. Nov 2014 A1
20160115759 Richards et al. Apr 2016 A1
20170114621 Holderman et al. Apr 2017 A1
20170254170 Mazyar et al. Sep 2017 A1
20170362922 Lazo et al. Dec 2017 A1
20180119526 Lopez et al. May 2018 A1
20190023979 Crews et al. Jan 2019 A1
20200408073 Weirich et al. Dec 2020 A1
20220003081 Kovalchuk Jan 2022 A1
20220003083 Sadana et al. Jan 2022 A1
20220003084 Kovalchuk et al. Jan 2022 A1
Foreign Referenced Citations (35)
Number Date Country
2969518 Jun 2016 CA
2343338 Oct 1999 CN
2903364 May 2007 CN
201794569 Apr 2011 CN
103620158 Mar 2014 CN
203476296 Mar 2014 CN
204267001 Apr 2015 CN
108086963 May 2018 CN
111499966 Aug 2020 CN
211201905 Aug 2020 CN
112459750 Mar 2021 CN
213450304 Jun 2021 CN
114412422 Apr 2022 CN
114542042 May 2022 CN
217421130 Sep 2022 CN
009070 Oct 2007 EA
1162055 Apr 2004 EP
2334899 Jun 2011 EP
2480752 Aug 2012 EP
2561179 Feb 2013 EP
2421527 Jun 2006 GB
2559973 Aug 2015 RU
2009045656 Apr 2009 WO
2012166234 Dec 2012 WO
2015041819 Mar 2015 WO
2015056260 Apr 2015 WO
2016032621 Mar 2016 WO
2016137439 Sep 2016 WO
2017155868 Sep 2017 WO
2019055166 Mar 2019 WO
2019083461 May 2019 WO
2020068409 Apr 2020 WO
2020172092 Aug 2020 WO
2021203799 Oct 2021 WO
2022081440 Apr 2022 WO
Non-Patent Literature Citations (16)
Entry
International Search Report and Written Opinion issued in the PCT Application PCT/US2020/018495, dated Jun. 12, 2020 (15 pages).
Carrejo, et al., “The Effects of Dynamic Loading on the Sand Management and Permeability of Shape Memory Polymer and Gravel Packs for Sand Management Applications”, SPE 143060—Brasil Offshore, Macae, Brazil, Jun. 14-17, 2011, 9 pages.
Crossland, et al., “A Bicontinuous Double Gyroid Hybrid Solar Cell”, Nano Letters, vol. 9 {8), 2009, pp. 2807-2812.
Wang, et al., “Co-Continuous Composite Materials for Stiffness, Strength, and Energy Dissipation”, Advanced Materials, vol. 23 (13), Apr. 5, 2011, pp. 1524-1529.
Wei, et al., “Review shape memory materials and hybrid composites for smart systems”, J. Mater. Sci., vol. 33, 1998, pp. 3763-3783.
Yuan, et al., “In-Situ Mechanical and Functional Behavior of Shape Memory Polymer Materials for Sand Management Applications”, SPE 143204—Brasil Offshore, Macae, Brazil, Jun. 14-17, 2011, 10 pages.
Zalusky, et al., “Ordered Nanoporous Polymers from Polystyrene-Polylactide Block Copolymers”, J. Am. Chem. Soc., vol. 124 (43), 2002, pp. 12761-12773.
International Search Report and Written Opinion issued in PCT/US2013/036100 dated Jul. 10, 2013, 13 pages.
Gibson, et al., “Cellular Solids: Structure & Properties”, Pergamon Press, Oxford, 1988, pp. 183.
Van Krevelen, et al., “Properties of Polymers”, 4th Edition, Elsevier B.V., New York, 2009, pp. 611.
Anonymous, “GeoFORM Conformable Sand Management System Improve reliability through total conformance,” Baker Hughes Incorporated, Brochure, 2011: 1-4.
Gibson et al., “(a) Linear elasticity,” Cellular solids Structure and properties—Second Edition, Cambridge University Press: New York, 1999: p. 183.
International Search Report and Written Opinion issued in the PCT Application PCT/US2023/010451 dated Apr. 27, 2023, 10 pages.
ASTM D1418—Standard Practice for Rubber and Rubber Latices—Nomenclature, originally approved in 1956 (3 pages).
International Search Report and Written Opinion issued in the PCT Application PCT/US2021/054334 dated Jan. 26, 2022 (11 pages).
International Preliminary Report on Patentability issued in PCT Application PCT/US2020/018495, dated Sep. 2, 2021 (10 pages).
Related Publications (1)
Number Date Country
20220127934 A1 Apr 2022 US
Provisional Applications (1)
Number Date Country
62808132 Feb 2019 US