CA2497948C - Method and stimulating oil and gas wells using deformable proppants - Google Patents
Method and stimulating oil and gas wells using deformable proppants Download PDFInfo
- Publication number
- CA2497948C CA2497948C CA2497948A CA2497948A CA2497948C CA 2497948 C CA2497948 C CA 2497948C CA 2497948 A CA2497948 A CA 2497948A CA 2497948 A CA2497948 A CA 2497948A CA 2497948 C CA2497948 C CA 2497948C
- Authority
- CA
- Canada
- Prior art keywords
- deformable
- proppant
- psi
- elastic modulus
- subterranean formation
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Active
Links
Classifications
-
- 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
-
- E—FIXED CONSTRUCTIONS
- E21—EARTH DRILLING; MINING
- E21B—EARTH DRILLING, e.g. DEEP DRILLING; OBTAINING OIL, GAS, WATER, SOLUBLE OR MELTABLE MATERIALS OR A SLURRY OF MINERALS FROM WELLS
- 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
Abstract
A method of fracturing using deformable proppants minimizes proppant pack damage, without compromising the fracturing fluid's proppant transport properties during pumping, by use of deformable proppants. Selection of proppant is dependent upon the mechanical properties of the formation rock. The strength of the deformable proppant is dependent upon the modulus of the formation rock being treated such that the proppant is capable of providing, at the very least, a minimum level of conductivity in in- situ stress environments. The maximum elastic modulus of the deformable proppant is less than the minimum modulus of the formation rock which is being treated. The method is particularly applicable in fracturing operations of subterranean reservoirs such as those comprised primarily of coal, chalk, limestone, dolomite, shale, siltstone, diatomite, etc.
Description
APPLICATION FOR PATENT
INVENTORS: HAROLD DEAN BRANNON, ALLAN RAY RICKARDS, CHRISTOPHER JOHN STEPHENSON, RUSSELL L.
MAHARIDGE
TITLE: METHOD OF STIMULATING OIL AND GAS WELLS USING
DEFORMABLE PROPPANTS
SPECIFICATION
Field of the Invention The invention relates to a method of fracturing using deformable proppants in order to minimize fines generation and proppant pack damage. The method of the invention has particular applicability in the fracturing of subterranean reservoirs such as those comprised primarily of coal, chalk, limestone, dolomite, shale, siltstone, diatomite, etc.
Background of the Invention Hydraulic fracturing is a common stimulation technique used to enhance production of fluids from subterranean formations. In a typical hydraulic fracturing treatment, fracturing treatment fluid containing a solid proppant is injected into the wellbore at pressures sufficient to create or enlarge a fracture in the reservoir. The proppant is deposited in the fracture, where it remains after the treatment is completed.
The proppant serves to hold the fracture open, thereby enhancing the ability of fluids to migrate from the formation to the wellbore through the fracture. Because well productivity depends on the ability of a fracture to conduct fluids from the formation to the wellbore, fracture conductivity is an important parameter in determining the degree of success of a hydraulic fracturing treatment.
Fracture conductivity may be reduced by small proppants or fines. In fracture conductivity testing using proppants of the prior art confined between sandstone cores, embedment of proppant into the core is frequently observed after exposure to elevated stress. In the process of embedment, spalling of fines from the rock is displaced into the proppant pack. Proppant pack conductivity damage from embedment results in loss of proppant pack width as the proppant embeds into the rock and proppant pack pore throats are plugged by displaced formation fines. The pack permeability is thereby reduced.
A second source of fines results from proppant crushing. Such fines are generated at the fracture-face to proppant pack interface as in situ closure stresses acting upon the fracture cause failure of the proppant, the formation rock, or both. Such stresses may cause the proppant to be compressed together such that fines are generated from the proppant pack and/or reservoir matrix. Further, fines composed of formation material (e.g., shale, sand, coal fines, etc.) may present similar problems and may be produced, for example, within the fractured formation due to stresses and forces applied to the formation during fracturing.
Proppant packs containing sand with a deformable proppant substantially reduce proppant crushing. Such proppant packs are disclosed in U.S. Patent Nos.
6,059,034 and 6,330,916. In addition to sand, such proppant packs contain deformable additives which act as a cushion and minimize the point stresses applied to the proppant and limit crushing of the sand. However, at elevated stress levels, the permeability and porosity levels of such proppant packs are compromised by embedment and spalling.
Alternate methods of reducing proppant pack damage and minimizing fines generation at increased stress levels have therefore been sought in order to increase the productivity of subterranean reservoirs.
Summary of the Invention The present invention relates to a method of minimizing proppant pack damage, without compromising the fracturing fluid's proppant transport properties during pumping, by use of deformable proppants. The method thereby improves the retained proppant pack permeability and, ultimately, the well's production. The method is particularly efficacious in minimizing plugging of proppant pack pore throats by migrating fines.
INVENTORS: HAROLD DEAN BRANNON, ALLAN RAY RICKARDS, CHRISTOPHER JOHN STEPHENSON, RUSSELL L.
MAHARIDGE
TITLE: METHOD OF STIMULATING OIL AND GAS WELLS USING
DEFORMABLE PROPPANTS
SPECIFICATION
Field of the Invention The invention relates to a method of fracturing using deformable proppants in order to minimize fines generation and proppant pack damage. The method of the invention has particular applicability in the fracturing of subterranean reservoirs such as those comprised primarily of coal, chalk, limestone, dolomite, shale, siltstone, diatomite, etc.
Background of the Invention Hydraulic fracturing is a common stimulation technique used to enhance production of fluids from subterranean formations. In a typical hydraulic fracturing treatment, fracturing treatment fluid containing a solid proppant is injected into the wellbore at pressures sufficient to create or enlarge a fracture in the reservoir. The proppant is deposited in the fracture, where it remains after the treatment is completed.
The proppant serves to hold the fracture open, thereby enhancing the ability of fluids to migrate from the formation to the wellbore through the fracture. Because well productivity depends on the ability of a fracture to conduct fluids from the formation to the wellbore, fracture conductivity is an important parameter in determining the degree of success of a hydraulic fracturing treatment.
Fracture conductivity may be reduced by small proppants or fines. In fracture conductivity testing using proppants of the prior art confined between sandstone cores, embedment of proppant into the core is frequently observed after exposure to elevated stress. In the process of embedment, spalling of fines from the rock is displaced into the proppant pack. Proppant pack conductivity damage from embedment results in loss of proppant pack width as the proppant embeds into the rock and proppant pack pore throats are plugged by displaced formation fines. The pack permeability is thereby reduced.
A second source of fines results from proppant crushing. Such fines are generated at the fracture-face to proppant pack interface as in situ closure stresses acting upon the fracture cause failure of the proppant, the formation rock, or both. Such stresses may cause the proppant to be compressed together such that fines are generated from the proppant pack and/or reservoir matrix. Further, fines composed of formation material (e.g., shale, sand, coal fines, etc.) may present similar problems and may be produced, for example, within the fractured formation due to stresses and forces applied to the formation during fracturing.
Proppant packs containing sand with a deformable proppant substantially reduce proppant crushing. Such proppant packs are disclosed in U.S. Patent Nos.
6,059,034 and 6,330,916. In addition to sand, such proppant packs contain deformable additives which act as a cushion and minimize the point stresses applied to the proppant and limit crushing of the sand. However, at elevated stress levels, the permeability and porosity levels of such proppant packs are compromised by embedment and spalling.
Alternate methods of reducing proppant pack damage and minimizing fines generation at increased stress levels have therefore been sought in order to increase the productivity of subterranean reservoirs.
Summary of the Invention The present invention relates to a method of minimizing proppant pack damage, without compromising the fracturing fluid's proppant transport properties during pumping, by use of deformable proppants. The method thereby improves the retained proppant pack permeability and, ultimately, the well's production. The method is particularly efficacious in minimizing plugging of proppant pack pore throats by migrating fines.
The deformable proppants used in the invention are softer than conventional proppants. As a result, they are capable of absorbing damaging stresses applied to the proppant pack. The proppant particulates act as cushions and such cushions are distributed uniformly throughout the proppant pack. Point stresses applied to the proppant are thereby minimized.
The strength of the deformable proppant used in the invention is dependent upon the hardness (or modulus) of the formation rock being treated. In particular, the modulus of the deformable proppant is such that the proppant is capable of providing, at the very least, a minimum level of conductivity in in situ stress environments.
Further, the maximum elastic modulus of the deformable proppant for use in the method of invention is less than the minimum modulus of the formation rock which is being treated.
Preferred as deformable proppants for use in the invention are:
(I.) naturally occurring materials, such as (a.) chipped, ground or crushed shells of nuts such as walnut, pecan, coconut, almond, ivory nut, brazil nut, etc.; (b.) chipped, ground or crushed seed shells (including fruit pits) of seeds of fruits such as plum, olive, peach, cherry, apricot, etc.; (c.) chipped, ground or crushed seed shells of other plants such as maize (e.g., corn cobs or corn kernels), etc.; and (d.) processed wood materials such as those derived from woods such as oak, hickory, walnut, poplar, mahogany, etc. Such proppants are strengthened or hardened with a protective coating or modifying agent which increases the ability of the material to resist deformation by strengthening or hardening the material (e.g., by increasing the elastic modulus of the naturally occurring material);
(II.) substantially spherical or beaded proppants of copolymers, such as polystyrene divnylbenzene, terpolymers, such as polystyrene/vinyl/divinyl benzene and acrylate-based terpolymers, and polymers of furfuryl derivatives, phenol formaldehyde, phenolic epoxy resins, polystyrene, methyl methacrylate, nylon, polycarbonates, polyethylene, polypropylene, polyvinylchloride, polyacrylonitrile-butadiene-styrene, polyurethane and mixtures thereof; and (III.) well treating aggregates composed of an organic lightweight material and a weight modifying agent.
The strength of the deformable proppant used in the invention is dependent upon the hardness (or modulus) of the formation rock being treated. In particular, the modulus of the deformable proppant is such that the proppant is capable of providing, at the very least, a minimum level of conductivity in in situ stress environments.
Further, the maximum elastic modulus of the deformable proppant for use in the method of invention is less than the minimum modulus of the formation rock which is being treated.
Preferred as deformable proppants for use in the invention are:
(I.) naturally occurring materials, such as (a.) chipped, ground or crushed shells of nuts such as walnut, pecan, coconut, almond, ivory nut, brazil nut, etc.; (b.) chipped, ground or crushed seed shells (including fruit pits) of seeds of fruits such as plum, olive, peach, cherry, apricot, etc.; (c.) chipped, ground or crushed seed shells of other plants such as maize (e.g., corn cobs or corn kernels), etc.; and (d.) processed wood materials such as those derived from woods such as oak, hickory, walnut, poplar, mahogany, etc. Such proppants are strengthened or hardened with a protective coating or modifying agent which increases the ability of the material to resist deformation by strengthening or hardening the material (e.g., by increasing the elastic modulus of the naturally occurring material);
(II.) substantially spherical or beaded proppants of copolymers, such as polystyrene divnylbenzene, terpolymers, such as polystyrene/vinyl/divinyl benzene and acrylate-based terpolymers, and polymers of furfuryl derivatives, phenol formaldehyde, phenolic epoxy resins, polystyrene, methyl methacrylate, nylon, polycarbonates, polyethylene, polypropylene, polyvinylchloride, polyacrylonitrile-butadiene-styrene, polyurethane and mixtures thereof; and (III.) well treating aggregates composed of an organic lightweight material and a weight modifying agent.
The method of the invention is particularly applicable in fracturing operations of soft subterranean reservoirs such as those comprised primarily of coal, chalk, limestone, dolomite, shale, siltstone, diatomite, etc.
Brief Description of the Drawings In order to more fully understand the drawings referred to in the detailed description of the present invention, a brief description of each drawing is presented, in which:
FIG. 1 (prior art) illustrates the formation of spalling and fines using non-deformable proppant proppants.
FIGs. 2(a) through 2(d) illustrate reduced formation spalling and fines by use of deformable proppants.
FIG. 3 is a schematic diagram of the proppant embedment test cell, discussed in the Examples.
FIGs. 4-8 are displacement curves at versus loads using deformable and non-deformable proppants. FIGS. 6-8 are prior art displacement curves showing results with non-deformable proppant and FIGs. 4-5 are displacement curves showing results with deformable proppants.
FIG. 9 (prior art) illustrates normal embedment using a non-deformable 20/40 bauxite proppant.
FIG. 10 illustrates the lack of embedment using a deformable proppant in accordance with the invention.
Detailed Description of the Preferred Embodiments The deformable proppants for use in the invention are capable of minimizing proppant pack damage and mitigating the formation of fines and crushed proppants during the fracturing process. After exposure of maximum applicable closure stresses, use of the deformable proppants of the invention exhibit little, if any, embedment of the proppants in the formation rock subjected to fracturing. Thus, such deformable proppants improve the retained proppant pack permeability. Productivity of the well is therefore enhanced.
Brief Description of the Drawings In order to more fully understand the drawings referred to in the detailed description of the present invention, a brief description of each drawing is presented, in which:
FIG. 1 (prior art) illustrates the formation of spalling and fines using non-deformable proppant proppants.
FIGs. 2(a) through 2(d) illustrate reduced formation spalling and fines by use of deformable proppants.
FIG. 3 is a schematic diagram of the proppant embedment test cell, discussed in the Examples.
FIGs. 4-8 are displacement curves at versus loads using deformable and non-deformable proppants. FIGS. 6-8 are prior art displacement curves showing results with non-deformable proppant and FIGs. 4-5 are displacement curves showing results with deformable proppants.
FIG. 9 (prior art) illustrates normal embedment using a non-deformable 20/40 bauxite proppant.
FIG. 10 illustrates the lack of embedment using a deformable proppant in accordance with the invention.
Detailed Description of the Preferred Embodiments The deformable proppants for use in the invention are capable of minimizing proppant pack damage and mitigating the formation of fines and crushed proppants during the fracturing process. After exposure of maximum applicable closure stresses, use of the deformable proppants of the invention exhibit little, if any, embedment of the proppants in the formation rock subjected to fracturing. Thus, such deformable proppants improve the retained proppant pack permeability. Productivity of the well is therefore enhanced.
The deformable proppants have particular applicability in fracturing operations of low permeability subterranean reservoirs such as those comprised primarily of coal, limestone, dolomite, shale, siltstone, diatomite, etc., known to be susceptible to fines generation due to their friable nature.
By "deformable" it is meant that the proppant particulates of the proppant pack substantially yield upon application of a minimum threshold level to point to point stress.
The in situ deformation of the proppants form multi-planar structures or networks and thus serve as a cushion to prevent grain-to-grain contact and absorb stress.
Such cushioning prevents the proppant from shattering or breaking due to stress (including stress induced by stress cycling). As a result, less fines are generated and permeability and/or conductivity is maintained. Such reduction in fines generation further permits the extension of the closure stress range in which the proppant pack may be used.
Selection of suitable deformable proppant for use in the invention is dependent upon the mechanical properties of the formation rock. In particular, the maximum modulus of the deformable proppant is selected such that it is less than the minimum modulus of the treated formation rock. The stress at which the proppant particulates are squeezed substantially flat is generally the maximum applicable stress for use of the proppant. Further, the modulus of the deformable proppant is such that the proppant is capable of providing, at the very least, a minimum level of conductivity in in situ stress environments.
Thus, the selected deformable proppant for use in the method of the invention may be selected to function in low to moderate stress environments (100 psi to 5,000 psi) as well as moderate to high stress environments (5,000 psi to 15,000 psi) while maintaining permeability and porosity of the fracture.
Thus, the deformable proppants used in the invention have an elastic modulus which is less than the maximum modulus of the formation rock, and yet exhibit sufficient integrity to resist gross proppant deformation. Typically, the deformable proppant has an elastic modulus of between about 500 psi and about 4,000,000 psi at in situ formation conditions. The requisite pack permeability is thereby maintained for a given in situ temperature and stress environment.
Since the selected deformable proppant is less hard than the rock of the subterranean formation, regardless of pressure or other physical parameters or mechanical properties placed on the formation, energy is absorbed by the proppant and not by the face of the rock when exposed to in-situ closure stresses. Thus, the proppant acts as a preferential cushion, absorbing the damaging stresses applied to the proppant pack via deformation of the deformable proppant particles. The cushion is distributed throughout the proppant pack, minimizing the point stresses applied to proppant particulates.
Examples of suitable deformable proppants include chipped, ground or crushed shells of nuts such as walnut, pecan, coconut, almond, ivory nut, brazil nut, etc. ; ground or crushed seed shells (including fruit pits) of seeds of fruits such as plum, olive, peach, cherry, apricot, etc.; ground or crushed seed shells of other plants such as maize (e.g., corn cobs or corn kernels), etc.; processed wood materials such as those derived from woods such as oak, hickory, walnut, poplar, mahogany, etc., including such woods that have been processed by grinding, chipping, or other form of particalization.
In one embodiment, specific gravity of such materials may range from about 0.4 to about 4.
Such materials may be otherwise processed to produce proppant material having any particle size or particle shape suitable for use in the method disclosed herein.
Such proppants may be optionally strengthened or hardened with a protective coating or modifying agent which increases the ability of the material to resist deformation by strengthening or hardening the material (e.g., by increasing the elastic modulus of the naturally occurring material). The resulting proppant has increased resistance (e.g., partial or complete resistance) to deformation under in situ formation or downhole conditions as compared to those proppants that have not been so modified.
Examples of suitable modifying agents include, but are not limited to, any compound or other material effective for modifying (e.g., crosslinking, coupling or otherwise reacting with) the proppant without degrading or otherwise damaging strength or hardness of the proppant, and/or without producing damaging by-products during modification that act to degrade or otherwise damage strength or hardness of the proppant (e.g., without liberating acids such as hydrochloric acid, organic acids, etc.).
By "deformable" it is meant that the proppant particulates of the proppant pack substantially yield upon application of a minimum threshold level to point to point stress.
The in situ deformation of the proppants form multi-planar structures or networks and thus serve as a cushion to prevent grain-to-grain contact and absorb stress.
Such cushioning prevents the proppant from shattering or breaking due to stress (including stress induced by stress cycling). As a result, less fines are generated and permeability and/or conductivity is maintained. Such reduction in fines generation further permits the extension of the closure stress range in which the proppant pack may be used.
Selection of suitable deformable proppant for use in the invention is dependent upon the mechanical properties of the formation rock. In particular, the maximum modulus of the deformable proppant is selected such that it is less than the minimum modulus of the treated formation rock. The stress at which the proppant particulates are squeezed substantially flat is generally the maximum applicable stress for use of the proppant. Further, the modulus of the deformable proppant is such that the proppant is capable of providing, at the very least, a minimum level of conductivity in in situ stress environments.
Thus, the selected deformable proppant for use in the method of the invention may be selected to function in low to moderate stress environments (100 psi to 5,000 psi) as well as moderate to high stress environments (5,000 psi to 15,000 psi) while maintaining permeability and porosity of the fracture.
Thus, the deformable proppants used in the invention have an elastic modulus which is less than the maximum modulus of the formation rock, and yet exhibit sufficient integrity to resist gross proppant deformation. Typically, the deformable proppant has an elastic modulus of between about 500 psi and about 4,000,000 psi at in situ formation conditions. The requisite pack permeability is thereby maintained for a given in situ temperature and stress environment.
Since the selected deformable proppant is less hard than the rock of the subterranean formation, regardless of pressure or other physical parameters or mechanical properties placed on the formation, energy is absorbed by the proppant and not by the face of the rock when exposed to in-situ closure stresses. Thus, the proppant acts as a preferential cushion, absorbing the damaging stresses applied to the proppant pack via deformation of the deformable proppant particles. The cushion is distributed throughout the proppant pack, minimizing the point stresses applied to proppant particulates.
Examples of suitable deformable proppants include chipped, ground or crushed shells of nuts such as walnut, pecan, coconut, almond, ivory nut, brazil nut, etc. ; ground or crushed seed shells (including fruit pits) of seeds of fruits such as plum, olive, peach, cherry, apricot, etc.; ground or crushed seed shells of other plants such as maize (e.g., corn cobs or corn kernels), etc.; processed wood materials such as those derived from woods such as oak, hickory, walnut, poplar, mahogany, etc., including such woods that have been processed by grinding, chipping, or other form of particalization.
In one embodiment, specific gravity of such materials may range from about 0.4 to about 4.
Such materials may be otherwise processed to produce proppant material having any particle size or particle shape suitable for use in the method disclosed herein.
Such proppants may be optionally strengthened or hardened with a protective coating or modifying agent which increases the ability of the material to resist deformation by strengthening or hardening the material (e.g., by increasing the elastic modulus of the naturally occurring material). The resulting proppant has increased resistance (e.g., partial or complete resistance) to deformation under in situ formation or downhole conditions as compared to those proppants that have not been so modified.
Examples of suitable modifying agents include, but are not limited to, any compound or other material effective for modifying (e.g., crosslinking, coupling or otherwise reacting with) the proppant without degrading or otherwise damaging strength or hardness of the proppant, and/or without producing damaging by-products during modification that act to degrade or otherwise damage strength or hardness of the proppant (e.g., without liberating acids such as hydrochloric acid, organic acids, etc.).
Examples of suitable types of modifying agents include compounds containing silicon-oxygen linkages, cyanate groups, epoxy groups, etc. Specific examples of suitable modifying agents include, but are not limited to, polyisocyanate-based compounds, silane-based compounds, siloxane-based compounds, epoxy-based combinations thereof, etc.
Protective coatings for coating at least a portion of the aforementioned proppant particulates include at least one of phenol formaldehyde resin, melamine formaldehyde resin, urethane resin, or a mixture thereof. Other optional coating compositions known in the art to be useful as hardeners for such materials (e.g., coating materials that function or serve to increase the elastic modulus of the material) may be also employed in conjunction or as an alternative to protective coatings, and may be placed underneath or on top of one or more protective coatings. Such protective and/or hardening coatings may be used in any combination suitable for imparting desired characteristics to the proppant, including in two or more multiple layers. In this regard successive layers of protective coatings, successive layers of hardening coatings, alternating layers of hardening and protective coatings, etc. are possible. Mixtures of protective and hardening coating materials may also be possible.
Protective coatings typically are present in an amount of from about 1% to about 20%, alternatively from about 2% to about 10% by weight of total weight of proppant particulates. The amount of protective coating affects the strength of the resulting proppant and thus its applicability for a given rock formation. For instance, in a reservoir having an elastic modulus of 3,000,000 at 175 F bottom hole static temperatures (BHST), and a closure stress of up to 6,000 psi, a relatively lightweight proppant having a thinner coating such as LitePropTM 125, a product of BJ Services Company, is suitable as deformable proppant. In a shallow coal bed methane application with reservoir elastic modulus of 500,000, BHST of 1000 F, and a closures stress of 300 psi, a deformable proppant having a thicker coatings, such as FlexsandTM LS, a product of BJ
Services Company, is often the preferred choice.
Further examples of such deformable proppants include substantially spherical or beaded proppants of copolymers, such as polystyrene divnylbenzene, terpolymers, such as polystyrene/vinyl/divinyl benzene and acrylate-based terpolymers, and polymers of furfuryl derivatives, phenol formaldehyde, phenolic epoxy resins, polystyrene, methyl methacrylate, nylon, polycarbonates, polyethylene, polypropylene, polyvinylchloride, polyacrylonitrile-butadiene-styrene, polyurethane and mixtures thereof.
Further, such copolymers may be reacted with a crosslinker, such as divinyl benzene. The amount of crosslinker employed is typically dependent on the targeted hardness and glass transition temperature of the resulting proppant. In this regard, any amount of crosslinker suitable for forming a deformable proppant may be employed. For example, beads containing less divinylbenzene crosslinker are preferred at lower formation closure stresses, as well as at lower temperatures. Thus, changing the percentage of divinylbenzene crosslinker present in polystyrene divinylbenzene beads from about 14% to about 4% to about 0.5% to about 0.3% changes the confined elastic modulus at standard conditions from about 100,000 psi to about 70,000 psi to about 50,000 psi to about 30,000 psi, respectively.
Further preferred as proppants for use in the invention are those relatively lightweight deformable proppants having an apparent specific gravity (ASG) (API RP
60) less than 2.65. In a preferred embodiment, the relatively lightweight proppants are ultra lightweight (ULW) proppants having an ASG less than or equal to 2.45.
Even more preferred are those ULW proppants having an ASG less than or equal to 2.25, preferably less than or equal to 2.0, more preferably less than or equal to 1.75, even more preferably less than or equal to 1.5, most preferably less than or equal to 1.25.
Included within such ULW proppants are well treating aggregates composed of an organic lightweight material and a weight modifying agent. The ASG of the organic lightweight material is either greater than or less than the ASG of the well treating aggregate depending on if the weight modifying agent is a weighting agent or weight reducing agent, respectively.
The aggregates are comprised of a continuous (external) phase composed of the organic lightweight material and a discontinuous (internal) phase composed of a weight modifying material. The amount of organic lightweight material in the aggregate is generally between from about 10 to about 90 percent by volume. The volume ratio of resin (continuous phase) to weight modifying agent (discontinuous phase) is generally between from about 20:80 to about 85:15, most preferably about 25:75. As an example, using an organic lightweight material having an ASG of 0.7 and a weight modifying agent, such as silica, having an ASG of 2.7, a 20:80 volume ratio would render an aggregate ASG of 2.20 and a 85:15 volume ratio would render an ASG of 1.0; a 75:25 volume ratio would render an ASG of 1.20.
The aggregate proppant diameter is typically approximately 850 microns. The average diameter of the weight modifying agent proppants is typically approximately 50 microns. The compressive strength of the aggregate is greater than the compressive strength of the organic lightweight material.
The organic lightweight material is preferably a polymeric material, such as a thermosetting resin, including polystyrene, a styrene-divinylbenzene copolymer, a polyacrylate, a polyalkylacrylate, a polyacrylate ester, a polyalkyl acrylate ester, a modified starch, a polyepoxide, a polyurethane, a polyisocyanate, a phenol formaldehyde resin, a furan resin, or a melamine formaldehyde resin. The ASG of the organic lightweight material generally less than or equal to 1.1. In a preferred embodiment, the ASG of the material is between about 0.7 to about 0.8.
In a preferred mode, the ASG of the well treating aggregate is at least about 0.35.
In a most preferred mode, the ASG of the well treating aggregate is at least about 0.70, more preferably 1.0, but not greater than about 2Ø
The weight modifying agent may be sand, glass, hematite, silica, sand, fly ash, aluminosilicate, and an alkali metal salt or trimanganese tetraoxide. In a preferred embodiment, the weight modifying agent is selected from finely ground sand, glass powder, glass spheres, glass beads, glass bubbles, ground glass, borosilicate glass or fiberglass. Further, the weight modifying agent may be a cation selected from alkali metal, alkaline earth metal, ammonium, manganese, and zinc and an anion selected from a halide, oxide, a carbonate, nitrate, sulfate, acetate and formate. For instance, the weight modifying agent may include calcium carbonate, potassium chloride, sodium chloride, sodium bromide, calcium chloride, barium sulfate, calcium bromide, zinc bromide, zinc formate, zinc oxide or a mixture thereof.
Glass bubbles and fly ash are the preferred components for the weight reducing agent.
Protective coatings for coating at least a portion of the aforementioned proppant particulates include at least one of phenol formaldehyde resin, melamine formaldehyde resin, urethane resin, or a mixture thereof. Other optional coating compositions known in the art to be useful as hardeners for such materials (e.g., coating materials that function or serve to increase the elastic modulus of the material) may be also employed in conjunction or as an alternative to protective coatings, and may be placed underneath or on top of one or more protective coatings. Such protective and/or hardening coatings may be used in any combination suitable for imparting desired characteristics to the proppant, including in two or more multiple layers. In this regard successive layers of protective coatings, successive layers of hardening coatings, alternating layers of hardening and protective coatings, etc. are possible. Mixtures of protective and hardening coating materials may also be possible.
Protective coatings typically are present in an amount of from about 1% to about 20%, alternatively from about 2% to about 10% by weight of total weight of proppant particulates. The amount of protective coating affects the strength of the resulting proppant and thus its applicability for a given rock formation. For instance, in a reservoir having an elastic modulus of 3,000,000 at 175 F bottom hole static temperatures (BHST), and a closure stress of up to 6,000 psi, a relatively lightweight proppant having a thinner coating such as LitePropTM 125, a product of BJ Services Company, is suitable as deformable proppant. In a shallow coal bed methane application with reservoir elastic modulus of 500,000, BHST of 1000 F, and a closures stress of 300 psi, a deformable proppant having a thicker coatings, such as FlexsandTM LS, a product of BJ
Services Company, is often the preferred choice.
Further examples of such deformable proppants include substantially spherical or beaded proppants of copolymers, such as polystyrene divnylbenzene, terpolymers, such as polystyrene/vinyl/divinyl benzene and acrylate-based terpolymers, and polymers of furfuryl derivatives, phenol formaldehyde, phenolic epoxy resins, polystyrene, methyl methacrylate, nylon, polycarbonates, polyethylene, polypropylene, polyvinylchloride, polyacrylonitrile-butadiene-styrene, polyurethane and mixtures thereof.
Further, such copolymers may be reacted with a crosslinker, such as divinyl benzene. The amount of crosslinker employed is typically dependent on the targeted hardness and glass transition temperature of the resulting proppant. In this regard, any amount of crosslinker suitable for forming a deformable proppant may be employed. For example, beads containing less divinylbenzene crosslinker are preferred at lower formation closure stresses, as well as at lower temperatures. Thus, changing the percentage of divinylbenzene crosslinker present in polystyrene divinylbenzene beads from about 14% to about 4% to about 0.5% to about 0.3% changes the confined elastic modulus at standard conditions from about 100,000 psi to about 70,000 psi to about 50,000 psi to about 30,000 psi, respectively.
Further preferred as proppants for use in the invention are those relatively lightweight deformable proppants having an apparent specific gravity (ASG) (API RP
60) less than 2.65. In a preferred embodiment, the relatively lightweight proppants are ultra lightweight (ULW) proppants having an ASG less than or equal to 2.45.
Even more preferred are those ULW proppants having an ASG less than or equal to 2.25, preferably less than or equal to 2.0, more preferably less than or equal to 1.75, even more preferably less than or equal to 1.5, most preferably less than or equal to 1.25.
Included within such ULW proppants are well treating aggregates composed of an organic lightweight material and a weight modifying agent. The ASG of the organic lightweight material is either greater than or less than the ASG of the well treating aggregate depending on if the weight modifying agent is a weighting agent or weight reducing agent, respectively.
The aggregates are comprised of a continuous (external) phase composed of the organic lightweight material and a discontinuous (internal) phase composed of a weight modifying material. The amount of organic lightweight material in the aggregate is generally between from about 10 to about 90 percent by volume. The volume ratio of resin (continuous phase) to weight modifying agent (discontinuous phase) is generally between from about 20:80 to about 85:15, most preferably about 25:75. As an example, using an organic lightweight material having an ASG of 0.7 and a weight modifying agent, such as silica, having an ASG of 2.7, a 20:80 volume ratio would render an aggregate ASG of 2.20 and a 85:15 volume ratio would render an ASG of 1.0; a 75:25 volume ratio would render an ASG of 1.20.
The aggregate proppant diameter is typically approximately 850 microns. The average diameter of the weight modifying agent proppants is typically approximately 50 microns. The compressive strength of the aggregate is greater than the compressive strength of the organic lightweight material.
The organic lightweight material is preferably a polymeric material, such as a thermosetting resin, including polystyrene, a styrene-divinylbenzene copolymer, a polyacrylate, a polyalkylacrylate, a polyacrylate ester, a polyalkyl acrylate ester, a modified starch, a polyepoxide, a polyurethane, a polyisocyanate, a phenol formaldehyde resin, a furan resin, or a melamine formaldehyde resin. The ASG of the organic lightweight material generally less than or equal to 1.1. In a preferred embodiment, the ASG of the material is between about 0.7 to about 0.8.
In a preferred mode, the ASG of the well treating aggregate is at least about 0.35.
In a most preferred mode, the ASG of the well treating aggregate is at least about 0.70, more preferably 1.0, but not greater than about 2Ø
The weight modifying agent may be sand, glass, hematite, silica, sand, fly ash, aluminosilicate, and an alkali metal salt or trimanganese tetraoxide. In a preferred embodiment, the weight modifying agent is selected from finely ground sand, glass powder, glass spheres, glass beads, glass bubbles, ground glass, borosilicate glass or fiberglass. Further, the weight modifying agent may be a cation selected from alkali metal, alkaline earth metal, ammonium, manganese, and zinc and an anion selected from a halide, oxide, a carbonate, nitrate, sulfate, acetate and formate. For instance, the weight modifying agent may include calcium carbonate, potassium chloride, sodium chloride, sodium bromide, calcium chloride, barium sulfate, calcium bromide, zinc bromide, zinc formate, zinc oxide or a mixture thereof.
Glass bubbles and fly ash are the preferred components for the weight reducing agent.
The aggregates are generally prepared by blending the organic lightweight material with weight modifying agent for a sufficient time in order to form a slurry or a mud which is then formed into sized proppants. Such proppants are then hardened by curing at temperatures ranging from about room temperature to about 200 C, preferably from about 50 C to about 150 C until the weight modifying agent hardens around the organic lightweight material.
In a preferred mode, the organic lightweight material forms a continuous phase, the weight modifying forming a discontinuous phase.
The ASG of the well treating aggregate is generally less than or equal to 2.0, preferably less than or equal to 1.5, to meet the pumping and/or downhole formation conditions of a particular application, such as hydraulic fracturing treatment, sand control treatment.
Such relatively lightweight proppants exhibit an elastic modulus of between about 500 psi and about 4,000,000 psi at formation conditions, more typically between about 5,000 psi and about 500,000 psi, more typically between about 5,000 psi and 200,000 psi at formation conditions, and most typically between about 7,000 psi and 150,000 psi at formation conditions. The elastic modulus of a well treating aggregate is substantially higher than the elastic modulus of the organic lightweight material or the weighting agent.
Where the weight modifying agent is a weighting agent, the ASG of the well treating aggregate is at least one and a half times the ASG of the organic lightweight material, the ASG of the well treating aggregate preferably being at least about 1.0, preferably at least about 1.25. In a preferred embodiment, the ASG of the organic lightweight material in such systems is approximately 0.7 and the ASG of the well treating aggregate is between from about 1.05 to about 1.20.
Where the weight modifying agent is a weight reducing agent, the ASG of the weight reducing agent is less than 1.0 and the ASG of the organic lightweight material is less than or equal to 1.1.
The weight modifying agent may be a weighting agent having a higher ASG than the organic lightweight material. The presence of the weighting agent renders a well treating aggregate having a ASG greater than the ASG of the organic lightweight material. Alternatively, the weight modifying agent may be a weight reducing agent having a lower ASG than the organic lightweight material. The presence of the weight reducing agent renders a well treating aggregate having a ASG less than the ASG of the organic lightweight material.
The amount of weight modifying agent in the well treating aggregate is such as to impart to the well treating aggregate the desired ASG. Typically, the amount of weight modifying agent in the well treating aggregate is between from about 15 to about 85 percent by volume of the well treating aggregate, most preferably approximately about 52 percent by volume. The sizes of the weight modifying agent are preferably between from about 10 microns to about 200 microns.
Further, a mixture of any of the deformable proppants may be utilized. As such, it is possible to use at least two materials having different deformation characteristics (such as differing values of elastic modulus). The first and second substantially deformable proppants, for example, may have different values of in situ elastic modulus.
For example, a first deformable proppant having an in situ elastic modulus of from about 500 psi to about 2,000,000 psi, may be combined with a second deformable proppant having an in situ elastic modulus of from about 500 psi to about 2,000,000 psi (alternatively from about 50,000 psi to about 150,000 psi), for example, for use in a relatively low stress closure stress environment. In another example, a first deformable proppant having an in situ elastic modulus of from about 2,000,000 psi to about 30,000,000 psi, may be combined with a second deformable proppant having an in situ elastic modulus of from about 500 psi to about 2,000,000 psi, for example, for use in a relatively high stress closure stress environment. Alternatively, the first and second substantially deformable materials may have similar or same values of in situ elastic modulus. Possible particle configurations include, but are not limited to, layered particles (such as concentrically layered particles), agglomerated particles, stratified particles, etc.
While the above proppants are generally referred to as substantially spherical, the deformable proppants for use in the invention may be any size or shape suitable for forming cushions in situ. For instance, in addition to being beaded or non-beaded, the deformable proppants for use in the invention may be non-spherical such as an elongated, tapered, egg, tear drop or oval shape or mixtures thereof. For instance, the proppants may have a shape that is cubic, bar-shaped (as in a hexahedron with a length greater than its width, and a width greater than its thickness), cylindrical, multi-faceted, irregular, or mixtures thereof. In addition, the deformable proppants may have a surface that is substantially roughened or irregular in nature or a surface that is substantially smooth in nature. Moreover, mixtures or blends of deformable proppants having differing, but suitable, shapes for use in the disclosed method further be employed.
In one embodiment, when deformable proppants having a cylindrical shape or an elongated beaded shape with a substantially uniform diameter, the proppant may have a maximum length aspect ratio equal to or less than about 5. As used herein, "maximum length based aspect ratio" means the maximum aspect ratio that may be obtained by dividing the length of the proppant by the minimum (or shortest) dimensional value that exists along any other axis (other than the length axis) taken through the center of mass of the proppant.
Any carrier fluid suitable for transporting a mixture of fracture proppant material into a formation fracture in a subterranean well may be employed with the deformable proppant including, but not limited to, carrier fluids comprising salt water, fresh water, liquid hydrocarbons, and/or nitrogen or other gases. Suitable carrier fluids include or may be used in combination with fluids have gelling agents, cross-linking agents, gel breakers, curable resins, hardening agents, solvents, surfactants, foaming agents, demulsifiers, buffers, clay stabilizers, acids, or mixtures thereof.
The deformable proppant may further be substantially neutrally buoyant in the carrier fluid. The term "substantially neutrally" refers to the condition wherein the proppant has an ASG sufficiently close to the ASG of the carrier fluid which allows pumping and satisfactory placement of the proppant into the formation. For instance, with the well treating aggregates, the ASG of the aggregate is selected so as to be close to the ASG of the carrier fluid. For example, the organic lightweight material may be treated with a weight modifying agent in such a way that the resulting well treating aggregate has a ASG close to the ASG of the carrier fluid so that it is neutrally buoyant or semi-buoyant in the fracturing fluid.
FIG. 1 illustrates the formation of spalling and fines using a non-deformable proppant 10 such as sand. The proppant is shown within the fracture 30 of formation 20.
In FIG. 1(b), embedment 40 of the non-deformable proppant into the exposed faces of the formation 20 creates formation spalling and the generation of fines 50. FIG.
1(c) illustrates the commencement of grain failure, at 60, of non-deformable proppant 10 as embedment increases. With increasing application of closure stress, increased embedment is evidenced, at 70, wherein the non-deformable proppant is crushed and formation fines form. The severity of embedment increases with the maximum applied closure stress.
FIGs. 2(a) through 2(d), in contrast, illustrate the effects encountered by use of deformable proppant 80. Initial placement of deformable proppant 80 is illustrated in FIG. 2(a) wherein the proppant is shown in fracture 30 of formation 20.
Increased pressure placed in the formation, illustrated in FIG. 2(b) and 2(c) causes limited embedment, at 90, and reduced formation spalling and generation of fines, at 100.
Further increased pressure, FIG. 2(d) demonstrates reduced fracture damage (less width loss and fines damage), at 110.
Deformable relatively lightweight proppants have particular applicability in minimizing coal fines generation that may result from "spalling" caused by embedment of the hydraulic fracture proppant into the exposed faces of the rock.
The following examples will illustrate the practice of the present invention in its preferred embodiments.
All parts are given in terms of weight units except as may otherwise be indicated.
LitePropTM 125, a product of BJ Services Company, is a proppant having an ASG
of 1.25.
EXAMPLES
The degree of embedment of 20/40 (mesh size) LitePropTM 125 and 20/40 Ottawa sand was determined by compressing a partial mono-layer (i.e., 43 particles/in2) of proppant against a shale core and measuring the displacement of a steel piston as a function of applied load, as exemplified in FIG. 3. The test, or embedment, cell was composed of a thick-walled stainless steel cylinder 10 and base plate 20, a 1-inch diameter steel piston 30, porous plate 40 on which the core sample 50 was placed. The proppant 60 was placed against core sample 50. Steel piston 30 pressed proppant 60 into core sample 50, and its displacement was used to infer proppant embedment.
Embedment was inferred by subtracting out the displacements of the core, test cell, and proppant compression. Mathematically, embedment (AXemb) was calculated from the following expression:
(AXemb) = (Axgross) - (Axsys) - (Axcore) - (Axprop) (1) Details of the steps taken to infer embedment were as follows:
1. Gross displacement versus load, Axgross, of a partial monolayer of proppant was measured the against the core sample.
2. Displacement of the embedment cell, Axsys, was then measured. Oxsys was parameterize by fitting either a logarithmic or polynomial function of 6th order through the data points.
3. The sum of displacements, AXprop + Oxsys, were measured of the embedment cell and compression of the partial monolayer of proppant. This was determined by pressing the proppant between steel platens.
4. The displacement of the embedment cell was then subtracted from the sum of displacements. This results in the displacement of the proppant, alone.
5. The sum of displacements of the core plus embedment cell, AXcore + OXsys, was then measured as a function of load. This data was parameterized by fitting either a logarithmic or polynomial function of 6th order through the data points.
6. The embedment was obtained by subtracting the displacements measured in Steps 5 and 4 from the displacement measured in Step 1.
The results demonstrate less embedment using LitePropTM 125 to Ottawa sand.
The degree of embedment of LitePropTM 125 and Ottawa sand loaded to 2000 lbs.
is set forth in Table I.
Table 1 Summary of Pro ant Embedment Results Measured Embedment 2000 lbs. Visual Observations Ottawa Sand Test 1 0.01 inches Embedment marks observed Test 3 0.0075 inches at surface. Many crushed Test 4 0.008 inches proppant grains. Some average 0.0085 inches grains fully embedded into surface.
LitePro TM 125 Some indentations Test 1 0.000 inches observed, but very shallow Test 2 0.00 inches depth. LitePropTM 125 average 0.00 inches grains were flattened into thin wafers.
FIGs. 4-8 display displacement over various loadings, wherein Curve "A" in each FIG. represents Axemb, Curve "B" represents Axprop, Curve "C" represents AXcore + Axsys and Curve "D" represents AXgross . FIGs. 4-5 are displacement curves showing the deformable LitePropTM 125 proppant and FIGs. 6-8 are displacement curves showing non-deformable Ottawa sand. The variation in response between different measurements is mainly due to differences in proppant shape among the LitePropTM 125 proppants. The variation in the slope of the displacement vs. load is due to the increasing cross-sectional area resulting from the deformation with increasing load. The slope's trend from steep to shallow with increasing load indicates increasing effective elastic modulus coupled with the change in cross-sectional area.
FIG. 9 is a photomicrograph at 4x magnification showing normal embedment when using Ottawa sand as (non-deformable) proppant. FIG. 10 is a photomicrograph at IOx magnification using the deformable LitePropTM proppant. FIG. 10, unlike FIG. 9, shows minimal embedment of LitePropTM 125. (FIGs. 4-5 demonstrate that embedment is so minimal that it could not be easily measured, as noted by the negative values over much of the load.) Thus, LitePropTM 125 embeds less than sand under identical conditions of proppant loading and applied stress.
From the foregoing, it will be observed that numerous variations and modifications may be effected without departing from the true spirit and scope of the novel concepts of the invention. It is intended that the specification, together with the examples, be considered exemplary only, with the scope and spirit of the invention being indicated by the claims which follow.
In a preferred mode, the organic lightweight material forms a continuous phase, the weight modifying forming a discontinuous phase.
The ASG of the well treating aggregate is generally less than or equal to 2.0, preferably less than or equal to 1.5, to meet the pumping and/or downhole formation conditions of a particular application, such as hydraulic fracturing treatment, sand control treatment.
Such relatively lightweight proppants exhibit an elastic modulus of between about 500 psi and about 4,000,000 psi at formation conditions, more typically between about 5,000 psi and about 500,000 psi, more typically between about 5,000 psi and 200,000 psi at formation conditions, and most typically between about 7,000 psi and 150,000 psi at formation conditions. The elastic modulus of a well treating aggregate is substantially higher than the elastic modulus of the organic lightweight material or the weighting agent.
Where the weight modifying agent is a weighting agent, the ASG of the well treating aggregate is at least one and a half times the ASG of the organic lightweight material, the ASG of the well treating aggregate preferably being at least about 1.0, preferably at least about 1.25. In a preferred embodiment, the ASG of the organic lightweight material in such systems is approximately 0.7 and the ASG of the well treating aggregate is between from about 1.05 to about 1.20.
Where the weight modifying agent is a weight reducing agent, the ASG of the weight reducing agent is less than 1.0 and the ASG of the organic lightweight material is less than or equal to 1.1.
The weight modifying agent may be a weighting agent having a higher ASG than the organic lightweight material. The presence of the weighting agent renders a well treating aggregate having a ASG greater than the ASG of the organic lightweight material. Alternatively, the weight modifying agent may be a weight reducing agent having a lower ASG than the organic lightweight material. The presence of the weight reducing agent renders a well treating aggregate having a ASG less than the ASG of the organic lightweight material.
The amount of weight modifying agent in the well treating aggregate is such as to impart to the well treating aggregate the desired ASG. Typically, the amount of weight modifying agent in the well treating aggregate is between from about 15 to about 85 percent by volume of the well treating aggregate, most preferably approximately about 52 percent by volume. The sizes of the weight modifying agent are preferably between from about 10 microns to about 200 microns.
Further, a mixture of any of the deformable proppants may be utilized. As such, it is possible to use at least two materials having different deformation characteristics (such as differing values of elastic modulus). The first and second substantially deformable proppants, for example, may have different values of in situ elastic modulus.
For example, a first deformable proppant having an in situ elastic modulus of from about 500 psi to about 2,000,000 psi, may be combined with a second deformable proppant having an in situ elastic modulus of from about 500 psi to about 2,000,000 psi (alternatively from about 50,000 psi to about 150,000 psi), for example, for use in a relatively low stress closure stress environment. In another example, a first deformable proppant having an in situ elastic modulus of from about 2,000,000 psi to about 30,000,000 psi, may be combined with a second deformable proppant having an in situ elastic modulus of from about 500 psi to about 2,000,000 psi, for example, for use in a relatively high stress closure stress environment. Alternatively, the first and second substantially deformable materials may have similar or same values of in situ elastic modulus. Possible particle configurations include, but are not limited to, layered particles (such as concentrically layered particles), agglomerated particles, stratified particles, etc.
While the above proppants are generally referred to as substantially spherical, the deformable proppants for use in the invention may be any size or shape suitable for forming cushions in situ. For instance, in addition to being beaded or non-beaded, the deformable proppants for use in the invention may be non-spherical such as an elongated, tapered, egg, tear drop or oval shape or mixtures thereof. For instance, the proppants may have a shape that is cubic, bar-shaped (as in a hexahedron with a length greater than its width, and a width greater than its thickness), cylindrical, multi-faceted, irregular, or mixtures thereof. In addition, the deformable proppants may have a surface that is substantially roughened or irregular in nature or a surface that is substantially smooth in nature. Moreover, mixtures or blends of deformable proppants having differing, but suitable, shapes for use in the disclosed method further be employed.
In one embodiment, when deformable proppants having a cylindrical shape or an elongated beaded shape with a substantially uniform diameter, the proppant may have a maximum length aspect ratio equal to or less than about 5. As used herein, "maximum length based aspect ratio" means the maximum aspect ratio that may be obtained by dividing the length of the proppant by the minimum (or shortest) dimensional value that exists along any other axis (other than the length axis) taken through the center of mass of the proppant.
Any carrier fluid suitable for transporting a mixture of fracture proppant material into a formation fracture in a subterranean well may be employed with the deformable proppant including, but not limited to, carrier fluids comprising salt water, fresh water, liquid hydrocarbons, and/or nitrogen or other gases. Suitable carrier fluids include or may be used in combination with fluids have gelling agents, cross-linking agents, gel breakers, curable resins, hardening agents, solvents, surfactants, foaming agents, demulsifiers, buffers, clay stabilizers, acids, or mixtures thereof.
The deformable proppant may further be substantially neutrally buoyant in the carrier fluid. The term "substantially neutrally" refers to the condition wherein the proppant has an ASG sufficiently close to the ASG of the carrier fluid which allows pumping and satisfactory placement of the proppant into the formation. For instance, with the well treating aggregates, the ASG of the aggregate is selected so as to be close to the ASG of the carrier fluid. For example, the organic lightweight material may be treated with a weight modifying agent in such a way that the resulting well treating aggregate has a ASG close to the ASG of the carrier fluid so that it is neutrally buoyant or semi-buoyant in the fracturing fluid.
FIG. 1 illustrates the formation of spalling and fines using a non-deformable proppant 10 such as sand. The proppant is shown within the fracture 30 of formation 20.
In FIG. 1(b), embedment 40 of the non-deformable proppant into the exposed faces of the formation 20 creates formation spalling and the generation of fines 50. FIG.
1(c) illustrates the commencement of grain failure, at 60, of non-deformable proppant 10 as embedment increases. With increasing application of closure stress, increased embedment is evidenced, at 70, wherein the non-deformable proppant is crushed and formation fines form. The severity of embedment increases with the maximum applied closure stress.
FIGs. 2(a) through 2(d), in contrast, illustrate the effects encountered by use of deformable proppant 80. Initial placement of deformable proppant 80 is illustrated in FIG. 2(a) wherein the proppant is shown in fracture 30 of formation 20.
Increased pressure placed in the formation, illustrated in FIG. 2(b) and 2(c) causes limited embedment, at 90, and reduced formation spalling and generation of fines, at 100.
Further increased pressure, FIG. 2(d) demonstrates reduced fracture damage (less width loss and fines damage), at 110.
Deformable relatively lightweight proppants have particular applicability in minimizing coal fines generation that may result from "spalling" caused by embedment of the hydraulic fracture proppant into the exposed faces of the rock.
The following examples will illustrate the practice of the present invention in its preferred embodiments.
All parts are given in terms of weight units except as may otherwise be indicated.
LitePropTM 125, a product of BJ Services Company, is a proppant having an ASG
of 1.25.
EXAMPLES
The degree of embedment of 20/40 (mesh size) LitePropTM 125 and 20/40 Ottawa sand was determined by compressing a partial mono-layer (i.e., 43 particles/in2) of proppant against a shale core and measuring the displacement of a steel piston as a function of applied load, as exemplified in FIG. 3. The test, or embedment, cell was composed of a thick-walled stainless steel cylinder 10 and base plate 20, a 1-inch diameter steel piston 30, porous plate 40 on which the core sample 50 was placed. The proppant 60 was placed against core sample 50. Steel piston 30 pressed proppant 60 into core sample 50, and its displacement was used to infer proppant embedment.
Embedment was inferred by subtracting out the displacements of the core, test cell, and proppant compression. Mathematically, embedment (AXemb) was calculated from the following expression:
(AXemb) = (Axgross) - (Axsys) - (Axcore) - (Axprop) (1) Details of the steps taken to infer embedment were as follows:
1. Gross displacement versus load, Axgross, of a partial monolayer of proppant was measured the against the core sample.
2. Displacement of the embedment cell, Axsys, was then measured. Oxsys was parameterize by fitting either a logarithmic or polynomial function of 6th order through the data points.
3. The sum of displacements, AXprop + Oxsys, were measured of the embedment cell and compression of the partial monolayer of proppant. This was determined by pressing the proppant between steel platens.
4. The displacement of the embedment cell was then subtracted from the sum of displacements. This results in the displacement of the proppant, alone.
5. The sum of displacements of the core plus embedment cell, AXcore + OXsys, was then measured as a function of load. This data was parameterized by fitting either a logarithmic or polynomial function of 6th order through the data points.
6. The embedment was obtained by subtracting the displacements measured in Steps 5 and 4 from the displacement measured in Step 1.
The results demonstrate less embedment using LitePropTM 125 to Ottawa sand.
The degree of embedment of LitePropTM 125 and Ottawa sand loaded to 2000 lbs.
is set forth in Table I.
Table 1 Summary of Pro ant Embedment Results Measured Embedment 2000 lbs. Visual Observations Ottawa Sand Test 1 0.01 inches Embedment marks observed Test 3 0.0075 inches at surface. Many crushed Test 4 0.008 inches proppant grains. Some average 0.0085 inches grains fully embedded into surface.
LitePro TM 125 Some indentations Test 1 0.000 inches observed, but very shallow Test 2 0.00 inches depth. LitePropTM 125 average 0.00 inches grains were flattened into thin wafers.
FIGs. 4-8 display displacement over various loadings, wherein Curve "A" in each FIG. represents Axemb, Curve "B" represents Axprop, Curve "C" represents AXcore + Axsys and Curve "D" represents AXgross . FIGs. 4-5 are displacement curves showing the deformable LitePropTM 125 proppant and FIGs. 6-8 are displacement curves showing non-deformable Ottawa sand. The variation in response between different measurements is mainly due to differences in proppant shape among the LitePropTM 125 proppants. The variation in the slope of the displacement vs. load is due to the increasing cross-sectional area resulting from the deformation with increasing load. The slope's trend from steep to shallow with increasing load indicates increasing effective elastic modulus coupled with the change in cross-sectional area.
FIG. 9 is a photomicrograph at 4x magnification showing normal embedment when using Ottawa sand as (non-deformable) proppant. FIG. 10 is a photomicrograph at IOx magnification using the deformable LitePropTM proppant. FIG. 10, unlike FIG. 9, shows minimal embedment of LitePropTM 125. (FIGs. 4-5 demonstrate that embedment is so minimal that it could not be easily measured, as noted by the negative values over much of the load.) Thus, LitePropTM 125 embeds less than sand under identical conditions of proppant loading and applied stress.
From the foregoing, it will be observed that numerous variations and modifications may be effected without departing from the true spirit and scope of the novel concepts of the invention. It is intended that the specification, together with the examples, be considered exemplary only, with the scope and spirit of the invention being indicated by the claims which follow.
Claims (251)
1. A method of fracturing a subterranean formation comprising:
introducing into the subterranean formation a fracturing fluid at a pressure sufficient to create or enlarge a fracture in the subterranean formation, wherein the fracturing fluid comprises a deformable proppant, the modulus of the deformable proppant being less than the modulus of the rock of the subterranean formation, the proppant being capable of providing at least a minimum level of conductivity;
allowing the subterranean formation to close such that the energy of the closure stress is absorbed by the deformable proppant and not by the face of the rock;
wherein embedment of the deformable proppant into the subterranean formation is minimized.
introducing into the subterranean formation a fracturing fluid at a pressure sufficient to create or enlarge a fracture in the subterranean formation, wherein the fracturing fluid comprises a deformable proppant, the modulus of the deformable proppant being less than the modulus of the rock of the subterranean formation, the proppant being capable of providing at least a minimum level of conductivity;
allowing the subterranean formation to close such that the energy of the closure stress is absorbed by the deformable proppant and not by the face of the rock;
wherein embedment of the deformable proppant into the subterranean formation is minimized.
2. The method of Claim 1, wherein the subterranean formation is susceptible to fines generation.
3. The method of Claim 2, wherein the subterranean formation is comprised primarily of coal, chalk, limestone, dolomite, shale, siltstone or diatomite.
4. The method of Claim 1, wherein the deformable proppant is a relatively lightweight proppant.
5. The method of Claim 1, wherein the deformable proppant is a relatively lightweight proppant selected from the group consisting of furan, furfuryl, phenol formaldehyde, phenolic epoxy, melamine formaldehyde resin, urethane resin or a mixture thereof.
6. The method of Claim 1, wherein the deformable proppant is a relatively lightweight proppant selected from the group consisting of polystyrene divinylbenzene, polystyrene/vinyl/divinyl benzene, acrylate-based terpolymer or a mixture thereof.
7. The method of Claim 1, wherein the deformable proppant has an elastic modulus of between about 500,000 psi and about 4,000,000 psi at in situ formation conditions.
8. The method of Claim 4, wherein the deformable proppant is a natural product selected from chipped, ground or crushed nut shells, seed shells, fruit pits and processed wood at least partially coated or hardened with a protective coating or modifying agent.
9. The method of Claim 8, wherein the natural product is selected from chipped, ground or crushed (i) walnut, pecan, coconut, almond, ivory or brazil nuts; (ii.) peach, plum, olive, cherry, or apricot seed shells.
10. The method of Claim 8, wherein the natural product is derived from oak, hickory, walnut, poplar or mahogany.
11. The method of Claim 1, wherein the deformable proppant is beaded, cubic, cylindrical, bar-shaped, multi-faceted, irregular or tapered in shape.
12. The method of Claim 1, wherein the deformable proppant has an elastic modulus of between about 500 to about 3,000,000 psi and is a natural product selected from (i.) chipped, ground or crushed walnut, pecan, coconut, almond, ivory or brazil nuts; (ii.) chipped, ground or crushed peach, plum, olive, cherry, or apricot seed shells;
or (iii.) derived from oak, hickory, walnut, poplar or mahogany.
or (iii.) derived from oak, hickory, walnut, poplar or mahogany.
13. The method of Claim 4, wherein the relatively lightweight proppant is an ultra lightweight (ULW) proppant.
14. The method of Claim 13, wherein the ULW proppant has an apparent specific gravity less than or equal to 1.25.
15. The method of Claim 1, wherein the deformable proppant is a substantially spherical or beaded proppant of polystyrene, methyl methacrylate, nylon, polycarbonates, polyethylene, polypropylene, polyvinylchloride, polypropylene, polyvinyl chloride or polyacrylonitrile-butadiene-styrene.
16. The method of Claim 15, wherein the deformable proppant is nylon.
17. The method of Claim 15, wherein the deformable proppant is relatively lightweight.
18. The method of Claim 1, wherein the deformable proppant is a well treating aggregate of an organic lightweight material and a weight modifying agent.
19. The method of Claim 18, wherein the organic lightweight material is selected from polystyrene, styrene-divinylbenzene copolymers, polyacrylates, polyalkyl acrylates, polyacrylate esters, polyalkyl acrylate esters, modified starches, polyepoxides, polyurethanes, polyisocyanates, phenol formaldehyde resins, furan resins and melamine formaldehyde resins.
20. The method of Claim 18, wherein the weight modifying agent is selected from finely ground sand, glass powder, glass spheres, glass beads, glass bubbles, ground glass, borosilicate glass and fiberglass.
21. The method of Claim 18, wherein the weight modifying agent is composed of (i.) a cation selected from alkali metal, alkaline earth metals, ammonium, manganese and zinc and (ii.) an anion selected from a halide, oxide, a carbonate, nitrate, sulfate, acetate and formate.
22. The method of Claim 1, wherein the deformable proppant has an apparent specific gravity less than or equal to 1.75.
23. The method of Claim 22, wherein the deformable proppant has an apparent specific gravity less than or equal to 1.5.
24. The method of Claim 23, wherein the deformable proppant has an apparent specific gravity less than or equal to 1.25.
25. The method of claim 4, wherein the relatively lightweight proppant has an elastic modulus of between about 5,000 and 500,000 psi.
26. The method of claim 25, wherein the relatively lightweight proppant has an elastic modulus of between about 5,000 and 200,000 psi.
27. The method of claim 26, wherein the relatively lightweight proppant has an elastic modulus of between about 7,000 and 150,000 psi.
28. The method of claim 7, wherein the deformable proppant has an elastic modulus of between about 50,000 psi and 150,000 psi at in situ formation conditions.
29. A method of fracturing a subterranean formation susceptible to fines generation comprising:
(a) contacting the subterranean formation with a deformable proppant at a pressure sufficient to initiate or enlarge a fracture, wherein the proppant has an apparent specific gravity less than or equal to 2.45; and (b) allowing the subterranean formation to close such that the energy of the closure stress is absorbed by the deformable proppant and not by the face of the rock wherein the fracture contains a partial monolayer of the deformable proppant and embedment of the deformable proppant into the subterranean formation is minimized and further wherein the fracture containing the partial monolayer of the deformable proppant is capable of providing at least a minimum level of conductivity at in-situ reservoir conditions.
(a) contacting the subterranean formation with a deformable proppant at a pressure sufficient to initiate or enlarge a fracture, wherein the proppant has an apparent specific gravity less than or equal to 2.45; and (b) allowing the subterranean formation to close such that the energy of the closure stress is absorbed by the deformable proppant and not by the face of the rock wherein the fracture contains a partial monolayer of the deformable proppant and embedment of the deformable proppant into the subterranean formation is minimized and further wherein the fracture containing the partial monolayer of the deformable proppant is capable of providing at least a minimum level of conductivity at in-situ reservoir conditions.
30. The method of Claim 29, wherein the deformable proppant has an apparent specific gravity less than or equal to 2Ø
31. The method of Claim 30, wherein the deformable proppant has an apparent specific gravity less than or equal to 1.75.
32. The method of Claim 31, wherein the deformable proppant has an apparent specific gravity less than or equal to 1.5.
33. The method of Claim 32, wherein the deformable proppant has an apparent specific gravity less than or equal to 1.25.
34. The method of any one of Claims 29-33, wherein the subterranean formation is selected from the group consisting of coal, chalk, limestone, dolomite, shale, siltstone and diatomite.
35. The method of any one of Claims 29-34, wherein the deformable proppant is selected from the group consisting of a furan, furfuryl, phenol formaldehyde, phenolic epoxy, melamine formaldehyde resin, urethane resin, polystyrene divinylbenzene, polystyrene/vinyl/divinyl benzene and acrylate-based terpolymer or a mixture thereof.
36. The method of any one of Claims 29-34, wherein the deformable proppant is a natural product selected from the group consisting of chipped, ground or crushed nut shells, seed shells, fruit pits and processed wood at least partially coated or hardened with a protective coating or modifying agent.
37. The method of Claim 36, wherein the natural product is selected from chipped, ground or crushed (i.) walnut, pecan, coconut, almond, ivory or brazil nuts; (ii.) peach, plum, olive, cherry, or apricot seed shells.
38. The method of any one of Claim 29-37, wherein the deformable proppant is beaded, cubic, cylindrical, bar-shaped, multi-faceted, irregular or tapered in shape.
39. The method of any one of Claims 29-38, wherein the deformable proppant is at least one member selected from the group consisting of polystyrene, methyl methacrylate, nylon, polycarbonates, polyethylene, polypropylene, polyvinylchloride, polypropylene, polyvinyl chloride, polyacrylonitrile-butadiene-styrene and mixtures thereof.
40. The method of Claim 39, wherein the deformable proppant is nylon.
41. The method of any one of Claims 29-40, wherein the deformable proppant has an elastic modulus of between about 500 psi and about 4,000,000 psi at in situ formation conditions
42. The method of any one of Claims 29-41, wherein the partial monolayer of the deformable proppant is capable of providing at least a minimum level of conductivity at in-situ reservoir stress conditions between from 100 psi to 15,000 psi.
43. The method of any one of Claims 29-42, wherein the deformable proppant comprises polystyrene divinylbenzene.
44. The method of any one of Claims 29-43, wherein step (a) comprises introducing into the subterranean formation particulates consisting essentially of the deformable proppant.
45. The method of any one of Claims 29-40 and 42-44, wherein the deformable proppant has an elastic modulus of between about 500,000 psi and about 4,000,000 psi at in situ formation conditions.
46. The method of claim 29, wherein the deformable proppant is a relatively lightweight proppant and has an elastic modulus of between about 5,000 and 500,000 psi.
47. The method of claim 46, wherein the relatively lightweight proppant has an elastic modulus of between about 5,000 and 200,000 psi.
48. The method of claim 47, wherein the relatively lightweight proppant has an elastic modulus of between about 7,000 and 150,000 psi.
49. The method of claim 45, wherein the deformable proppant has an elastic modulus of between about 50,000 psi and 150,000 psi at in situ formation conditions.
50. A method of fracturing a soft subterranean formation comprising:
(a) introducing into the soft subterranean formation a deformable proppant having an elastic modulus of between from about 500 to about 3,000,000 psi, wherein the modulus of the deformable proppant is less than the modulus of the subterranean formation and further wherein the soft subterranean formation is selected from the group consisting of coal, chalk, limestone, dolomite, shale, siltstone and diatomite; and (b) allowing the subterranean formation to close such that the energy of the closure stress is absorbed by the deformable proppant and not by the face of the rock;
(c) wherein embedment of the deformable proppant into the reservoir is minimized.
(a) introducing into the soft subterranean formation a deformable proppant having an elastic modulus of between from about 500 to about 3,000,000 psi, wherein the modulus of the deformable proppant is less than the modulus of the subterranean formation and further wherein the soft subterranean formation is selected from the group consisting of coal, chalk, limestone, dolomite, shale, siltstone and diatomite; and (b) allowing the subterranean formation to close such that the energy of the closure stress is absorbed by the deformable proppant and not by the face of the rock;
(c) wherein embedment of the deformable proppant into the reservoir is minimized.
51. The method of Claim 50, wherein the deformable proppant is selected from the group consisting of a furan, furfuryl, phenol formaldehyde, phenolic epoxy, melamine formaldehyde resin, urethane resin, polystyrene divinylbenzene, polystyrene/vinyl/divinyl benzene and acrylate-based terpolymer or a mixture thereof.
52. The method of Claim 50, wherein the deformable proppant is a natural product selected from the group consisting of chipped, ground or crushed nut shells, seed shells, fruit pits and processed wood at least partially coated or hardened with a protective coating or modifying agent.
53. The method of Claim 52, wherein the natural product is selected from chipped, ground or crushed (i.) walnut, pecan, coconut, almond, ivory or brazil nuts; (ii.) peach, plum, olive, cherry, or apricot seed shells.
54. The method of Claim 52, wherein the natural product is derived from oak, hickory, walnut, poplar or mahogany.
55. The method of Claim 50, wherein the deformable proppant is beaded, cubic, cylindrical, bar-shaped, multi-faceted, irregular or tapered in shape.
56. The method of Claim 50, wherein the deformable proppant is at least one member selected from the group consisting of polystyrene, methyl methacrylate, nylon, polycarbonates, polyethylene, polypropylene, polyvinylchloride, polypropylene, polyvinyl chloride, polyacrylonitrile-butadiene-styrene and mixtures thereof.
57. The method of Claim 56, wherein the deformable proppant is nylon.
58. The method of Claim 50, wherein the deformable proppant has an apparent specific gravity less than or equal to 1.75.
59. The method of Claim 58, wherein the deformable proppant has an apparent specific gravity less than or equal to 1.5.
60. The method of Claim 59, wherein the deformable proppant has an apparent specific gravity less than or equal to 1.25.
61. The method of any one of Claims 50-60, wherein the fracture contains a partial monolayer of the deformable proppant, which is capable of providing at least a minimum level of conductivity at in-situ reservoir stress conditions between from 100 psi to 15,000 psi.
62. The method of any one of Claims 50, 51 and 56-61, wherein the deformable proppant comprises polystyrene divinylbenzene.
63. The method of any one of Claims 50-62, wherein step (a) comprises introducing into the subterranean formation particulates consisting essentially of the deformable proppant.
64. The method of any one of Claims 50-63, wherein the deformable proppant has an elastic modulus above about 500,000 psi at in situ formation conditions.
65. The method of any one of Claims 50-64 wherein the fracture contains a partial monolayer of the deformable proppant and further wherein the fracture containing the partial monolayer of the deformable proppant is capable of providing at least a minimum level of conductivity at in-situ reservoir conditions.
66. The method of any one of Claims 50-65, wherein the deformable proppant is introduced into the formation at a pressure sufficient to create or enlarge a fracture.
67. The method of claim 50, wherein the deformable proppant is a relatively lightweight proppant and has an elastic modulus of between about 5,000 and 500,000 psi.
68. The method of claim 67, wherein the relatively lightweight proppant has an elastic modulus of between about 5,000 and 200,000 psi.
69. The method of claim 68, wherein the relatively lightweight proppant has an elastic modulus of between about 7,000 and 150,000 psi.
70. The method of claim 50, wherein the deformable proppant has an elastic modulus of between about 50,000 psi and 150,000 psi at in situ formation conditions.
71. A method of fracturing a subterranean formation surrounding an oil or gas well which comprises:
(a) contacting the subterranean formation with a deformable proppant at a pressure sufficient to initiate or enlarge a fracture, the proppant comprising an organic lightweight material and a weight modifying agent, the modulus of the deformable proppant being less than the modulus of the rock of the subterranean formation; and (b) allowing the subterranean formation to close such that the energy of the closure stress is absorbed by the deformable proppant and not by the face of the rock wherein embedment of the deformable proppant into the subterranean formation is minimized.
(a) contacting the subterranean formation with a deformable proppant at a pressure sufficient to initiate or enlarge a fracture, the proppant comprising an organic lightweight material and a weight modifying agent, the modulus of the deformable proppant being less than the modulus of the rock of the subterranean formation; and (b) allowing the subterranean formation to close such that the energy of the closure stress is absorbed by the deformable proppant and not by the face of the rock wherein embedment of the deformable proppant into the subterranean formation is minimized.
72. The method of Claim 71, wherein the deformable proppant is comprised of a continuous phase composed of the organic lightweight material and a discontinuous phase composed of a weight modifying material.
73. The method of Claim 71, wherein the amount of organic lightweight material in the deformable proppant is generally between from about 10 to about 90 percent by volume.
74. The method of Claim 72, wherein the organic lightweight material is a polymeric material selected from the group consisting of polystyrene, a styrene-divinylbenzene copolymer, a polyacrylate, a polyalkylacrylate, a polyacrylate ester, a polyalkyl acrylate ester, a modified starch, a polyepoxide, a polyurethane, a polyisocyanate, a phenol formaldehyde resin, a furan resin and a melamine formaldehyde resin.
75. The method of Claim 72, wherein the weight modifying agent is selected from the group consisting of sand, glass, hematite, silica, sand, fly ash, aluminosilicate, trimanganese tetraoxide and an alkali metal salt.
76. The method of Claim 72, wherein the weight modifying agent is selected from the group consisting of finely ground sand, glass powder, glass spheres, glass beads, glass bubbles, ground glass, borosilicate glass and fiberglass.
77. The method of Claim 72, wherein the weight modifying agent contains a cation selected from the group consisting of an alkali metal, alkaline earth metal, ammonium, manganese and zinc and an anion selected from the group consisting of a halide, oxide, a carbonate, nitrate, sulfate, acetate and formate.
78. The method of Claim 72, wherein the weight modifying agent is selected from the group consisting of calcium carbonate, potassium chloride, sodium chloride, sodium bromide, calcium chloride, barium sulfate, calcium bromide, zinc bromide, zinc formate, zinc oxide, glass bubbles and fly ash or a mixture thereof.
79. The method of Claim 71, wherein the deformable proppant is at least one member selected from the group consisting of polystyrene, methyl methacrylate, nylon, polycarbonates, polyethylene, polypropylene, polyvinylchloride, polypropylene, polyvinyl chloride, polyacrylonitrile-butadiene-styrene and mixtures thereof.
80. The method of Claim 79, wherein the deformable proppant is nylon.
81. The method of Claim 72, wherein the deformable proppant has an apparent specific gravity less than or equal to 1.75.
82. The method of Claim 81, wherein the deformable proppant has an apparent specific gravity less than or equal to 1.5.
83. The method of Claim 82, wherein the deformable proppant has an apparent specific gravity less than or equal to 1.25.
84. The method of any one of Claims 71-83, wherein the fracture contains a partial monolayer of the deformable proppant which is capable of providing at least a minimum level of conductivity at in-situ reservoir stress conditions between from 100 psi to 15,000 psi.
85. The method of any one of Claims 71-84, wherein the deformable proppant comprises polystyrene divinylbenzene.
86. The method of any one of Claims 71-85, wherein step (a) comprises introducing into the subterranean formation particulates consisting essentially of the deformable proppant.
87. The method of any one of Claims 71-86, wherein the deformable proppant has an elastic modulus between about 500 psi and about 4,000,000 psi at in situ formation conditions.
88. The method of Claim 87, wherein the deformable proppant has an elastic modulus above about 500,000 psi at in situ formation conditions.
89. The method of any one of Claims 71-88, wherein the fracture contains a partial monolayer of the deformable proppant and further wherein the fracture containing the partial monolayer of the deformable proppant is capable of providing at least a minimum level of conductivity at in-situ reservoir conditions.
90. The method of claim 71, wherein the deformable proppant is a relatively lightweight proppant and has an elastic modulus of between about 5,000 and 500,000 psi.
91. The method of claim 90, wherein the relatively lightweight proppant has an elastic modulus of between about 5,000 and 200,000 psi.
92. The method of claim 91, wherein the relatively lightweight proppant has an elastic modulus of between about 7,000 and 150,000 psi.
93. The method of claim 87, wherein the deformable proppant has an elastic modulus of between about 50,000 psi and 150,000 psi at in situ formation conditions.
94. A method of fracturing a subterranean formation susceptible to fines generation comprising:
(a) introducing into the subterranean formation particulates consisting essentially of deformable proppants, wherein the particulates have an apparent specific gravity less than or equal to 2.45; and (b) allowing the subterranean formation to close on the created partial monolayer such that the energy of the closure stress is absorbed by the deformable proppants and not by the face of the rock wherein said formation contains a partial monolayer of said particulates and embedment of the deformable proppants into the subterranean formation is minimized and further wherein the fracture containing the partial monolayer of deformable proppants is capable of providing at least a minimum level of conductivity at in-situ reservoir conditions.
(a) introducing into the subterranean formation particulates consisting essentially of deformable proppants, wherein the particulates have an apparent specific gravity less than or equal to 2.45; and (b) allowing the subterranean formation to close on the created partial monolayer such that the energy of the closure stress is absorbed by the deformable proppants and not by the face of the rock wherein said formation contains a partial monolayer of said particulates and embedment of the deformable proppants into the subterranean formation is minimized and further wherein the fracture containing the partial monolayer of deformable proppants is capable of providing at least a minimum level of conductivity at in-situ reservoir conditions.
95. The method of Claim 94, wherein the deformable proppants have an apparent specific gravity less than or equal to 2Ø
96. The method of Claim 95, wherein the deformable proppants have an apparent specific gravity less than or equal to 1.75.
97. The method of Claim 96, wherein the deformable proppants have an apparent specific gravity less than or equal to 1.5.
98. The method of Claim 97, wherein the deformable proppants have an apparent specific gravity less than or equal to 1.25.
99. The method of Claim 94, wherein the subterranean formation is selected from the group consisting of coal, chalk, limestone, dolomite, shale, siltstone and diatomite.
100. The method of Claim 94, wherein the deformable proppants are at least one member selected from the group consisting of a furan, furfuryl, phenol formaldehyde, phenolic epoxy, melamine formaldehyde resin, urethane resin, polystyrene divinylbenzene, polystyrene/vinyl/divinyl benzene and acrylate-based terpolymer or a mixture thereof.
101. The method of Claim 100, wherein the deformable proppants are at least one member of a natural product selected from the group consisting of chipped, ground or crushed nut shells, seed shells, fruit pits and processed wood at least partially coated or hardened with a protective coating or modifying agent.
102. The method of Claim 101, wherein the natural product is selected from chipped, ground or crushed (i.) walnut, pecan, coconut, almond, ivory or brazil nuts;
(ii.) peach, plum, olive, cherry, or apricot seed shells.
(ii.) peach, plum, olive, cherry, or apricot seed shells.
103. The method of Claim 94, wherein the deformable proppants are beaded, cubic, cylindrical, bar-shaped, multi-faceted, irregular or tapered in shape.
104. The method of any one of Claims 94-103, wherein the partial monolayer of the deformable proppant is capable of providing at least a minimum level of conductivity at in-situ reservoir stress conditions between from 100 psi to 15,000 psi.
105. The method of any one of Claims 94-99, 103 and 104, wherein the deformable proppant comprises polystyrene divinylbenzene.
106. The method of any one of Claims 94-105, wherein step (a) comprises introducing into the subterranean formation particulates consisting essentially of the deformable proppant.
107. The method of any one of Claims 94-106, wherein the deformable proppant has an elastic modulus between about 500 psi and about 4,000,000 psi at in situ formation conditions.
108. The method of Claim 107, wherein the deformable proppant has an elastic modulus above about 500,000 psi at in situ formation conditions.
109. The method of any one of Claims 94-108 wherein the partial monolayer of the deformable proppant is capable of providing at least a minimum level of conductivity at in-situ reservoir conditions.
110. The method of any one of Claims 94-109, wherein the deformable proppant is introduced into the formation at a pressure sufficient to create or enlarge a fracture.
111. The method of claim 94, wherein the deformable proppant is a relatively lightweight proppant and has an elastic modulus of between about 5,000 and 500,000 psi.
112. The method of claim 111, wherein the relatively lightweight proppant has an elastic modulus of between about 5,000 and 200,000 psi.
113. The method of claim 112, wherein the relatively lightweight proppant has an elastic modulus of between about 7,000 and 150,000 psi.
114. The method of claim 107, wherein the deformable proppant has an elastic modulus of between about 50,000 psi and 150,000 psi at in situ formation conditions.
115. A method of fracturing a soft subterranean formation comprising:
A. introducing into the soft subterranean formation a deformable proppant, wherein the deformable proppant consists essentially of either:
(a) particulates having an apparent specific gravity less than or equal to 2.45; or (b) particulates having an apparent specific gravity less than or equal to 2.45 having a coating or modifying agent which increases the resistance of the particulates to deformation and further wherein the deformable proppant has an elastic modulus of between from about 500 to about 3,000,000 psi, wherein the modulus of the deformable proppant is less than the modulus of the subterranean formation and further wherein the soft subterranean formation is selected from the group consisting of coal, chalk, limestone, dolomite, shale, siltstone and diatomite; and allowing the subterranean formation to close such that the energy of the closure stress is absorbed by the deformable proppant and not by the face of the rock;
wherein embedment of the deformable proppant into the reservoir is minimized.
A. introducing into the soft subterranean formation a deformable proppant, wherein the deformable proppant consists essentially of either:
(a) particulates having an apparent specific gravity less than or equal to 2.45; or (b) particulates having an apparent specific gravity less than or equal to 2.45 having a coating or modifying agent which increases the resistance of the particulates to deformation and further wherein the deformable proppant has an elastic modulus of between from about 500 to about 3,000,000 psi, wherein the modulus of the deformable proppant is less than the modulus of the subterranean formation and further wherein the soft subterranean formation is selected from the group consisting of coal, chalk, limestone, dolomite, shale, siltstone and diatomite; and allowing the subterranean formation to close such that the energy of the closure stress is absorbed by the deformable proppant and not by the face of the rock;
wherein embedment of the deformable proppant into the reservoir is minimized.
116. The method of Claim 115, wherein the soft subterranean formation is selected from the group consisting of coal, chalk, siltstone and diatomite.
117. The method of Claim 115, wherein the deformable proppant is selected from the group consisting of a furan, furfuryl, phenol formaldehyde, phenolic epoxy, melamine formaldehyde resin, urethane resin, polystyrene divinylbenzene, polystyrene/vinyl/divinyl benzene and acrylate-based terpolymer or a mixture thereof.
118. The method of Claim 115, wherein the deformable proppant is a natural product selected from the group consisting of chipped, ground or crushed nut shells, seed shells, fruit pits and processed wood at least partially coated or hardened with a protective coating or modifying agent.
119. The method of Claim 118, wherein the natural product is selected from chipped, ground or crushed (i.) walnut, pecan, coconut, almond, ivory or brazil nuts;
(ii.) peach, plum, olive, cherry, or apricot seed shells.
(ii.) peach, plum, olive, cherry, or apricot seed shells.
120. The method of Claim 118, wherein the natural product is derived from oak, hickory, walnut, poplar or mahogany.
121. The method of Claim 115, wherein the deformable proppant is beaded, cubic, cylindrical, bar-shaped, multi-faceted, irregular or tapered in shape.
122. The method of any one of Claims 115-121, wherein the fracture contains a partial monolayer of the deformable proppant which is capable of providing at least a minimum level of conductivity at in-situ reservoir stress conditions between from 100 psi to 15,000 psi.
123. The method of any one of Claims 115, 116 and 121-122, wherein the deformable proppant comprises polystyrene divinylbenzene.
124. The method of any one of Claims 115-123, wherein step (a) comprises introducing into the subterranean formation particulates consisting essentially of the deformable proppant.
125. The method of any one of Claims 115-124, wherein the deformable proppant has an elastic modulus above about 500,000 psi at in situ formation conditions.
126. The method of any one of Claims 115-125 wherein the fracture contains a partial monolayer of the deformable proppant and further wherein the fracture containing the partial monolayer of the deformable proppant is capable of providing at least a minimum level of conductivity at in-situ reservoir conditions.
127. The method of any one of Claims 115-126 wherein the deformable particulates have an elastic modulus of between about 500,000 psi and about 2,000,000 psi at in situ formation conditions.
128. The method of any one of Claims 115-127, wherein the deformable proppant is introduced into the formation at a pressure sufficient to create or enlarge a fracture.
129. The method of any one of Claims 95-128, wherein the deformable proppants have an apparent specific gravity less than or equal to 2Ø
130. The method of Claim 129, wherein the deformable proppants have an apparent specific gravity less than or equal to 1.75.
131. The method of Claim 130, wherein the deformable proppants have an apparent specific gravity less than or equal to 1.5.
132. The method of Claim 131, wherein the deformable proppants have an apparent specific gravity less than or equal to 1.25.
133. The method of claim 115, wherein the deformable proppant is a relatively lightweight proppant and has an elastic modulus of between about 5,000 and 500,000 psi.
134. The method of claim 133, wherein the relatively lightweight proppant has an elastic modulus of between about 5,000 and 200,000 psi.
135. The method of claim 134, wherein the relatively lightweight proppant has an elastic modulus of between about 7,000 and 150,000 psi.
136. The method of claim 115, wherein the deformable proppant has an elastic modulus of between about 50,000 psi and 150,000 psi at in situ formation conditions.
137. A method of fracturing a subterranean formation surrounding an oil or gas well which comprises:
(a) introducing into the subterranean formation a deformable proppant, wherein the deformable proppant consists essentially of:
(i) an aggregate of an organic lightweight material and a weight modifying, agent; or (ii) an aggregate of an organic lightweight material and weight modifying agent, the aggregate having a coating or modifying agent which increases the resistance of the aggregate to deformation the modulus of the deformable proppant being less than the modulus of the rock of the subterranean formation; and (b) allowing the subterranean formation to close such that the energy of the closure stress is absorbed by the deformable proppant and not by the face of the rock wherein embedment of the deformable proppant into the subterranean formation is minimized.
(a) introducing into the subterranean formation a deformable proppant, wherein the deformable proppant consists essentially of:
(i) an aggregate of an organic lightweight material and a weight modifying, agent; or (ii) an aggregate of an organic lightweight material and weight modifying agent, the aggregate having a coating or modifying agent which increases the resistance of the aggregate to deformation the modulus of the deformable proppant being less than the modulus of the rock of the subterranean formation; and (b) allowing the subterranean formation to close such that the energy of the closure stress is absorbed by the deformable proppant and not by the face of the rock wherein embedment of the deformable proppant into the subterranean formation is minimized.
138. The method of Claim 137, wherein the deformable proppant is comprised of a continuous phase composed of the organic lightweight material and a discontinuous phase composed of a weight modifying material.
139. The method of Claim 137, wherein the amount of organic lightweight material in the aggregate is generally between from about 10 to about 90 percent by volume.
140. The method of Claim 137, wherein the organic lightweight material is a polymeric material selected from the group consisting of polystyrene, a styrene-divinylbenzene copolymer, a polyacrylate, a polyalkylacrylate, a polyacrylate ester, a polyalkyl acrylate ester, a modified starch, a polyepoxide, a polyurethane, a polyisocyanate, a phenol formaldehyde resin, a furan resin and a melamine formaldehyde resin.
141. The method of Claim 137, wherein the weight modifying agent is selected from the group consisting of sand, glass, hematite, silica, sand, fly ash, aluminosilicate, trimanganese tetraoxide and an alkali metal salt.
142. The method of Claim 137, wherein the weight modifying agent is selected from the group consisting of finely ground sand, glass powder, glass spheres, glass beads, glass bubbles, ground glass, borosilicate glass and fiberglass.
143. The method of Claim 137, wherein the weight modifying agent contains a cation selected from the group consisting of an alkali metal, alkaline earth metal, ammonium, manganese and zinc and an anion selected from the group consisting of a halide, oxide, a carbonate, nitrate, sulfate, acetate and formate.
144. The method of Claim 137, wherein the weight modifying agent is selected from the group consisting of calcium carbonate, potassium chloride, sodium chloride, sodium bromide, calcium chloride, barium sulfate, calcium bromide, zinc bromide, zinc formate, zinc oxide, glass bubbles and fly ash or a mixture thereof.
145. The method of any one of Claims 137-144, wherein the fracture contains a partial monolayer of the deformable proppant which is capable of providing at least a minimum level of conductivity at in-situ reservoir stress conditions between from 100 psi to 15,000 psi.
146. The method of Claim 137, wherein the deformable proppant comprises polystyrene divinylbenzene.
147. The method of any one of Claims 137-146, wherein step (a) comprises introducing into the subterranean formation particulates consisting essentially of the deformable proppant.
148. The method of any one of Claims 137-147, wherein the deformable proppant has an elastic modulus between about 500 psi and about 4,000,000 psi at in situ formation conditions.
149. The method of claim 148, wherein the deformable proppant has an elastic modulus above about 500,000 psi at in situ formation conditions.
150. The method of any one of Claims 137-149, wherein the fracture contains a partial monolayer of the deformable proppant and further wherein the fracture containing the partial monolayer of the deformable proppant is capable of providing at least a minimum level of conductivity at in-situ reservoir conditions.
151. The method of any one of Claims 137-150 wherein the deformable particulates have an elastic modulus of between about 500,000 psi and about 2,000,000 psi at in situ formation conditions.
152. The method of any one of Claims 137-151, wherein the deformable proppant is introduced into the formation at a pressure sufficient to create or enlarge a fracture.
153. The method of any one of Claims 137-152, wherein the deformable proppants have an apparent specific gravity less than or equal to 2Ø
154. The method of Claim 153, wherein the deformable proppants have an apparent specific gravity less than or equal to 1.75.
155. The method of Claim 154, wherein the deformable proppants have an apparent specific gravity less than or equal to 1.5.
156. The method of Claim 155, wherein the deformable proppants have an apparent specific gravity less than or equal to 1.25.
157. The method of claim 137, wherein the deformable proppant is a relatively lightweight proppant and has an elastic modulus of between about 5,000 and 500,000 psi.
158. The method of claim 157, wherein the relatively lightweight proppant has an elastic modulus of between about 5,000 and 200,000 psi.
159. The method of claim 158, wherein the relatively lightweight proppant has an elastic modulus of between about 7,000 and 150,000 psi.
160. The method of claim 151, wherein the deformable proppant has an elastic modulus of between about 50,000 psi and 150,000 psi at in situ formation conditions.
161. A method of fracturing a subterranean formation susceptible to fines generation comprising:
(A) introducing into the subterranean formation a fracturing fluid at a pressure sufficient to create or enlarge a fracture in the subterranean formation, wherein the fracturing fluid comprises a deformable proppant, wherein the deformable proppant consists essentially of either:
(a) particulates having an apparent specific gravity less than or equal to 2.45;
or (b) particulates having an apparent specific gravity less than or equal to 2.45 having a coating or modifying agent which increases the resistance of the particulates to deformation, the modulus of the deformable proppant being less than the modulus of the rock of the subterranean formation, the proppant being capable of providing at least a minimum level of conductivity;
(B) allowing the subterranean formation to close such that the energy of the closure stress is absorbed by the deformable proppant and not by the face of the rock;
wherein embedment of the deformable proppant into the subterranean formation is minimized.
(A) introducing into the subterranean formation a fracturing fluid at a pressure sufficient to create or enlarge a fracture in the subterranean formation, wherein the fracturing fluid comprises a deformable proppant, wherein the deformable proppant consists essentially of either:
(a) particulates having an apparent specific gravity less than or equal to 2.45;
or (b) particulates having an apparent specific gravity less than or equal to 2.45 having a coating or modifying agent which increases the resistance of the particulates to deformation, the modulus of the deformable proppant being less than the modulus of the rock of the subterranean formation, the proppant being capable of providing at least a minimum level of conductivity;
(B) allowing the subterranean formation to close such that the energy of the closure stress is absorbed by the deformable proppant and not by the face of the rock;
wherein embedment of the deformable proppant into the subterranean formation is minimized.
162. The method of Claim 161, wherein the subterranean formation is comprised primarily of coal, chalk, limestone, dolomite, shale, siltstone or diatomite.
163. The method of Claim 161, wherein the apparent specific gravity of the deformable proppant is less than or equal to 2.25.
164. The method of Claim 161, wherein the deformable proppant is selected from the group consisting of furan, furfuryl, phenol formaldehyde, phenolic epoxy, melamine formaldehyde resin, urethane resin or a mixture thereof.
165. The method of Claim 161, wherein the deformable proppant is selected from the group consisting of polystyrene divinylbenzene, polystyrene/vinyl/divinyl benzene, acrylate-based terpolymer or a mixture thereof.
166. The method of Claim 161, wherein the deformable proppant has an elastic modulus of between about 500,000 psi and about 4,000,000 psi at in situ formation conditions.
167. The method of Claim 161, wherein the deformable proppant is a natural product selected from chipped, ground or crushed nut shells, seed shells, fruit pits and processed wood at least partially coated or hardened with a protective coating or modifying agent.
168. The method of Claim 167, wherein the natural product is selected from chipped, ground or crushed (i.) walnut, pecan, coconut, almond, ivory or brazil nuts;
(ii.) peach, plum, olive, cherry, or apricot seed shells.
(ii.) peach, plum, olive, cherry, or apricot seed shells.
169. The method of Claim 167, wherein the natural product is derived from oak, hickory, walnut, poplar or mahogany.
170. The method of Claim 161, wherein the deformable proppant is beaded, cubic, cylindrical, bar-shaped, multi-faceted, irregular or tapered in shape.
171. The method of Claim 163, wherein the deformable proppant has an apparent specific gravity less than or equal to 2Ø
172. The method of Claim 163, wherein the deformable proppant is selected from the group consisting of furan, furfuryl, phenol formaldehyde, phenolic epoxy, melamine formaldehyde resin, urethane resin, polystyrene divinylbenzene, polystyrene/vinyl/divinyl benzene, acrylate-based terpolymer, polystyrene, methyl methacrylate, polycarbonates, polyethylene, polypropylene, polyvinylchloride, polypropylene, polyvinyl chloride, polyacrylonitrile-butadiene-styrene and mixtures thereof.
173. The method of Claim 161, wherein the deformable proppant is a natural product selected from chipped, ground or crushed nut shells, seed shells, fruit pits and processed wood at least partially coated or hardened with a protective coating or modifying agent.
174. The method of any one of Claims 161-173, wherein the fracture contains a partial monolayer of the deformable proppant which is capable of providing at least a minimum level of conductivity at in-situ reservoir stress conditions between from 100 psi to 15,000 psi.
175. The method of any one of Claims 161, 163, 170, 171 and 174, wherein the deformable proppant comprises polystyrene divinylbenzene.
176. The method of any one of Claims 161-75, wherein step (a) comprises introducing into the subterranean formation particulates consisting essentially of the deformable proppant.
177. The method of any one of Claims 161-176, wherein the deformable particulates have an elastic modulus of between about 500,000 psi and about 2,000,000 psi at in situ formation conditions.
178. The method of any one of Claims 161-177, wherein the fracture contains a partial monolayer of the deformable proppant and further wherein the fracture containing the partial monolayer of the deformable proppant is capable of providing at least a minimum level of conductivity at in-situ reservoir conditions.
179. The method of Claim 161, wherein the deformable proppants have an apparent specific gravity less than or equal to 2Ø
180. The method of Claim 179, wherein the deformable proppants have an apparent specific gravity less than or equal to 1.75.
181. The method of Claim 180, wherein the deformable proppants have an apparent specific gravity less than or equal to 1.5.
182. The method of Claim 181, wherein the deformable proppants have an apparent specific gravity less than or equal to 1.25.
183. The method of claim 161, wherein the deformable proppant is a relatively lightweight proppant and has an elastic modulus of between about 5,000 and 500,000 psi.
184. The method of claim 183, wherein the relatively lightweight proppant has an elastic modulus of between about 5,000 and 200,000 psi.
185. The method of claim 184, wherein the relatively lightweight proppant has an elastic modulus of between about 7,000 and 150,000 psi.
186. The method of claim 166, wherein the deformable proppant has an elastic modulus of between about 50,000 psi and 150,000 psi at in situ formation conditions.
187. A method of fracturing a subterranean formation comprising:
(a) introducing into the subterranean formation a fracturing fluid at a pressure sufficient to create or enlarge a fracture in the subterranean formation, wherein the fracturing fluid comprises a deformable proppant, the modulus of the deformable proppant being less than the modulus of the rock of the subterranean formation, wherein the proppant has an apparent specific gravity between from about 1.0 and about 1.2; and (b) allowing the subterranean formation to close such that the energy of the closure stress is absorbed by the deformable proppant and not by the face of the rock wherein a fracture contains a partial monolayer of the deformable proppant and embedment of the deformable proppant into the subterranean formation is minimized and further wherein the fracture containing the partial monolayer of deformable proppant is capable of providing at least a minimum level of conductivity at in-situ reservoir conditions.
(a) introducing into the subterranean formation a fracturing fluid at a pressure sufficient to create or enlarge a fracture in the subterranean formation, wherein the fracturing fluid comprises a deformable proppant, the modulus of the deformable proppant being less than the modulus of the rock of the subterranean formation, wherein the proppant has an apparent specific gravity between from about 1.0 and about 1.2; and (b) allowing the subterranean formation to close such that the energy of the closure stress is absorbed by the deformable proppant and not by the face of the rock wherein a fracture contains a partial monolayer of the deformable proppant and embedment of the deformable proppant into the subterranean formation is minimized and further wherein the fracture containing the partial monolayer of deformable proppant is capable of providing at least a minimum level of conductivity at in-situ reservoir conditions.
188. The method of Claim 187, wherein the deformable proppants are at least one member selected from the group consisting of polystyrene, methyl methacrylate, nylon, polycarbonates, polyethylene, polypropylene, polyvinylchloride, polypropylene, polyvinyl chloride, polyacrylonitrile-butadiene-styrene and mixtures thereof.
189. The method of Claim 188, wherein the deformable proppant is nylon.
190. The method of Claim 187, wherein the deformable proppant comprises polystyrene divinylbenzene.
191. The method of any one of Claims 187-190, wherein step (a) comprises introducing into the subterranean formation particulates consisting essentially of the deformable proppant.
192. The method of any one of Claims 187-191, wherein the deformable proppant has an elastic modulus of between about 500 psi and about 4,000,000 psi at in situ formation conditions.
193. The method of Claim 192, wherein the deformable proppant has an elastic modulus of above about 500,000 psi at in situ formation conditions.
194. The method of claim 187, wherein the deformable proppant is a relatively lightweight proppant and has an elastic modulus of between about 5,000 and 500,000 psi.
195. The method of claim 194, wherein the relatively lightweight proppant has an elastic modulus of between about 5,000 and 200,000 psi.
196. The method of claim 195, wherein the relatively lightweight proppant has an elastic modulus of between about 7,000 and 150,000 psi.
197. The method of claim 192, wherein the deformable proppant has an elastic modulus of between about 50,000 psi and 150,000 psi at in situ formation conditions.
198. A method of fracturing a subterranean formation susceptible to fines generation comprising:
(a) introducing deformable proppants into the subterranean formation at a pressure sufficient to hydraulically create or enlarge fractures in the formation, wherein the deformable proppants consist essentially of deformable particulates which have an elastic modulus of between about 500 psi and about 4,000,000 psi at in situ formation conditions and which have an apparent specific gravity less than or equal to 2.45 wherein fractures are created or enlarged and the created or enlarged fractures have a partial monolayer of said deformable proppants; and (b) allowing the subterranean formation to close on the created partial monolayer such that the energy of the closure stress is absorbed by the deformable proppants and not by the face of the rock wherein embedment of the deformable proppants into the subterranean formation is minimized and further wherein the fracture containing the partial monolayer of deformable proppants is capable of providing at least a minimum level of conductivity at in-situ reservoir conditions.
(a) introducing deformable proppants into the subterranean formation at a pressure sufficient to hydraulically create or enlarge fractures in the formation, wherein the deformable proppants consist essentially of deformable particulates which have an elastic modulus of between about 500 psi and about 4,000,000 psi at in situ formation conditions and which have an apparent specific gravity less than or equal to 2.45 wherein fractures are created or enlarged and the created or enlarged fractures have a partial monolayer of said deformable proppants; and (b) allowing the subterranean formation to close on the created partial monolayer such that the energy of the closure stress is absorbed by the deformable proppants and not by the face of the rock wherein embedment of the deformable proppants into the subterranean formation is minimized and further wherein the fracture containing the partial monolayer of deformable proppants is capable of providing at least a minimum level of conductivity at in-situ reservoir conditions.
199. The method of Claim 198, wherein the deformable particulates have an apparent specific gravity less than or equal to 2Ø
200. The method of Claim 199, wherein the deformable particulates have an apparent specific gravity less than or equal to 1.75.
201. The method of Claim 200, wherein the deformable particulates have an apparent specific gravity less than or equal to 1.5.
202. The method of Claim 201, wherein the deformable particulates have an apparent specific gravity less than or equal to 1.25.
203. The method of Claim 198, wherein the subterranean formation is selected from the group consisting of coal, chalk, limestone, dolomite, shale, siltstone and diatomite.
204. The method of Claim 198, wherein the deformable particulates are at least one member selected from the group consisting of a furan, furfuryl, phenol formaldehyde, phenolic epoxy, melamine formaldehyde resin, urethane resin, polystyrene divinylbenzene, polystyrene/vinyl/divinyl benzene and acrylate-based terpolymer or a mixture thereof.
205. The method of Claim 204, wherein the deformable particulates are at least one member of a natural product selected from the group consisting of chipped, ground or crushed nut shells, seed shells, fruit pits and processed wood at least partially coated or hardened with a protective coating or modifying agent.
206. The method of Claim 205, wherein the natural product is selected from chipped, ground or crushed (i.) walnut, pecan, coconut, almond, ivory or brazil nuts;
(ii.) peach, plum, olive, cherry, or apricot seed shells.
(ii.) peach, plum, olive, cherry, or apricot seed shells.
207. The method of Claim 198, wherein the deformable particulates are beaded, cubic, cylindrical, bar-shaped, multi-faceted, irregular or tapered in shape.
208. The method of any one of Claims 198-203 and 207, wherein the deformable proppant comprises polystyrene divinylbenzene.
209. The method of claim 198, wherein the deformable proppant is a relatively lightweight proppant and has an elastic modulus of between about 5,000 and 500,000 psi.
210. The method of claim 209, wherein the relatively lightweight proppant has an elastic modulus of between about 5,000 and 200,000 psi.
211. The method of claim 210, wherein the relatively lightweight proppant has an elastic modulus of between about 7,000 and 150,000 psi.
212. The method of claim 198, wherein the deformable proppant has an elastic modulus of between about 50,000 psi and 150,000 psi at in situ formation conditions.
213. A method of fracturing a subterranean formation susceptible to fines generation comprising:
introducing into the subterranean formation at a pressure sufficient to create or enlarge a fracture in the subterranean formation a fracturing fluid containing deformable particulates;
hydraulically creating or enlarging a fracture in the formation, wherein a proppant pack of the deformable particulates is deposited in the fracture, wherein the deformable particulates of the proppant pack consist essentially of either:
(a) deformable particulates having an apparent specific gravity less than or equal to 2.45; or (b) deformable particulates having an apparent specific gravity less than or equal to 2.45 having a coating or modifying agent which increases the resistance of the deformable particulates to deformation, the modulus of the deformable-particulates being less than the modulus of the rock of the subterranean formation, the particulates being capable of providing at least a minimum level of conductivity;
allowing the subterranean formation to close such that the energy of the closure stress is absorbed by the deformable proppant pack and not by the face of the rock;
wherein embedment of the deformable particulates into the subterranean formation is minimized.
introducing into the subterranean formation at a pressure sufficient to create or enlarge a fracture in the subterranean formation a fracturing fluid containing deformable particulates;
hydraulically creating or enlarging a fracture in the formation, wherein a proppant pack of the deformable particulates is deposited in the fracture, wherein the deformable particulates of the proppant pack consist essentially of either:
(a) deformable particulates having an apparent specific gravity less than or equal to 2.45; or (b) deformable particulates having an apparent specific gravity less than or equal to 2.45 having a coating or modifying agent which increases the resistance of the deformable particulates to deformation, the modulus of the deformable-particulates being less than the modulus of the rock of the subterranean formation, the particulates being capable of providing at least a minimum level of conductivity;
allowing the subterranean formation to close such that the energy of the closure stress is absorbed by the deformable proppant pack and not by the face of the rock;
wherein embedment of the deformable particulates into the subterranean formation is minimized.
214. The method of Claim 213, wherein the apparent specific gravity of the deformable particulates is less than or equal to 2.25.
215. The method of Claim 213, wherein the deformable particulates are selected from the group consisting of furan, furfuryl, phenol formaldehyde, phenolic epoxy, melamine formaldehyde resin, urethane resin and mixtures thereof.
216. The method of Claim 213, wherein the deformable particulates are selected from the group consisting of polystyrene divinylbenzene, polystyrene/vinyl/divinyl benzene, acrylate-based terpolymer and mixtures thereof.
217. The method of Claim 213, wherein the deformable particulates have an elastic modulus of between about 500,000 psi and about 2,000,000 psi at in situ formation conditions.
218. The method of Claim 213, wherein the deformable particulates are a natural product selected from chipped, ground or crushed nut shells, seed shells, fruit pits and processed wood at least partially coated or hardened with a protective coating or modifying agent.
219. The method of Claim 218, wherein the natural product is selected from chipped, ground or crushed (i.) walnut, pecan, coconut, almond, ivory or brazil nuts;
(ii.) peach, plum, olive, cherry, or apricot seed shells.
(ii.) peach, plum, olive, cherry, or apricot seed shells.
220. The method of Claim 213, wherein the natural product is derived from oak, hickory, walnut, poplar or mahogany.
221. The method of Claim 213, wherein the deformable particulates are beaded, cubic, cylindrical, bar-shaped, multi-faceted, irregular or tapered in shape.
222. The method of Claim 221, wherein the deformable particulates have an apparent specific gravity less than or equal to 2Ø
223. The method of Claim 222, wherein the deformable particulates have an apparent specific gravity less than or equal to 1.25.
224. The method of Claim 213, wherein the deformable particulates are selected from the group consisting of furan, furfuryl, phenol formaldehyde, phenolic epoxy, melamine formaldehyde resin, urethane resin, polystyrene divinylbenzene, polystyrene/vinyl/divinyl benzene, acrylate-based terpolymer, polystyrene, methyl methacrylate, polycarbonates, polyethylene, polypropylene, polyvinylchloride, polypropylene, polyvinyl chloride, polyacrylonitrile-butadiene-styrene and mixtures thereof.
225. The method of Claim 213, wherein the deformable particulates are a natural product selected from chipped, ground or crushed nut shells, seed shells, fruit pits and processed wood at least partially coated or hardened with a protective coating or modifying agent.
226. The method of any one of Claims 213-225, wherein the partial monolayer of the deformable proppant is capable of providing at least a minimum level of conductivity at in-situ reservoir stress conditions between from 100 psi to 15,000 psi.
227. The method of any one of Claims 213, 214, 216, 217, 221-223 and 226 wherein the deformable proppant comprises polystyrene divinylbenzene.
228. The method of any one of Claims 213-227, wherein step (a) comprises introducing into the subterranean formation particulates consisting essentially of the deformable proppant.
229. The method of claim 213, wherein the deformable proppant is a relatively lightweight proppant and has an elastic modulus of between about 5,000 and 500,000 psi.
230. The method of claim 229, wherein the relatively lightweight proppant has an elastic modulus of between about 5,000 and 200,000 psi.
231. The method of claim 230, wherein the relatively lightweight proppant has an elastic modulus of between about 7,000 and 150,000 psi.
232. The method of claim 213, wherein the deformable proppant has an elastic modulus of between about 50,000 psi and 150,000 psi at in situ formation conditions.
233. A method of fracturing a subterranean formation comprising:
(a) introducing into the subterranean formation a fracturing fluid at a pressure sufficient to hydraulically create or enlarge a fracture in the formation, wherein the fracturing fluid comprises deformable proppants having an apparent specific gravity less than or equal to 1.25, wherein the deformable proppants are composed only of particulates which are deformable;
(b) allowing the subterranean formation to close such that the energy of the closure stress is absorbed by the deformable particulates and not by the face of the rock, wherein the permeability and porosity of the fracture is maintained by the deformable particulates while embedment of the deformable particulates into the subterranean formation is minimized while the fracture is held open by the deformable proppants.
(a) introducing into the subterranean formation a fracturing fluid at a pressure sufficient to hydraulically create or enlarge a fracture in the formation, wherein the fracturing fluid comprises deformable proppants having an apparent specific gravity less than or equal to 1.25, wherein the deformable proppants are composed only of particulates which are deformable;
(b) allowing the subterranean formation to close such that the energy of the closure stress is absorbed by the deformable particulates and not by the face of the rock, wherein the permeability and porosity of the fracture is maintained by the deformable particulates while embedment of the deformable particulates into the subterranean formation is minimized while the fracture is held open by the deformable proppants.
234. The method of Claim 233, wherein the deformable particulates are nylon.
235. The method of Claim 233, wherein the deformable proppants in the created or enlarged fracture are in the form of a partial monolayer.
236. The method of Claim 233, wherein the deformable particulates have an elastic modulus of between about 500,000 psi and about 2,000,000 psi at in situ formation conditions.
237. The method of Claim 233, wherein the subterranean formation is comprised primarily of coal, chalk, limestone, dolomite, shale, siltstone or diatomite.
238. The method of Claim 233, wherein the deformable particulates are substantially spherical or beaded.
239. The method of Claim 238, wherein the deformable particulates are beaded.
240. The method of Claim 233, wherein the deformable proppant further comprises a weight modifying agent.
241. The method of Claim 240, wherein the weight modifying agent is selected from the group consisting of sand, glass, hematite, silica, fly ash, aluminosilicate, alkali metal salts and trimanganese tetraoxide.
242. The method of Claim 241, wherein the weight modifying agent is fly ash.
243. The method of any one of Claims 233-242, wherein the partial monolayer of the deformable proppant is capable of providing at least a minimum level of conductivity at in-situ reservoir stress conditions between from 100 psi to 15,000 psi.
244. The method of any one of Claims 233 and 235-239, wherein the deformable proppant comprises polystyrene divinylbenzene.
245. The method of any one of Claims 233-244, wherein step (a) comprises introducing into the subterranean formation particulates consisting essentially of the deformable proppant.
246. The method of any one of Claims 233-245, wherein the deformable proppant has an elastic modulus of between about 500,000 psi and about 4,000,000 psi at in situ formation conditions.
247. The method of any one of Claims 233-245, wherein the deformable proppant has an elastic modulus of between about 500,000 psi and about 2,000,000 psi at in situ formation conditions.
248. The method of claim 233, wherein the deformable proppant is a relatively lightweight proppant and has an elastic modulus of between about 5,000 and 500,000 psi.
249. The method of claim 248, wherein the relatively lightweight proppant has an elastic modulus of between about 5,000 and 200,000 psi.
250. The method of claim 249, wherein the relatively lightweight proppant has an elastic modulus of between about 7,000 and 150,000 psi.
251. The method of claim 247, wherein the deformable proppant has an elastic modulus of between about 50,000 psi and 150,000 psi at in situ formation conditions.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CA2715597A CA2715597C (en) | 2005-01-12 | 2005-02-22 | Method of stimulating oil and gas wells using deformable proppants |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US11/034,388 US7322411B2 (en) | 2005-01-12 | 2005-01-12 | Method of stimulating oil and gas wells using deformable proppants |
US11/034,388 | 2005-01-12 |
Related Child Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CA2715597A Division CA2715597C (en) | 2005-01-12 | 2005-02-22 | Method of stimulating oil and gas wells using deformable proppants |
Publications (2)
Publication Number | Publication Date |
---|---|
CA2497948A1 CA2497948A1 (en) | 2006-07-12 |
CA2497948C true CA2497948C (en) | 2011-05-10 |
Family
ID=36652104
Family Applications (2)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CA2497948A Active CA2497948C (en) | 2005-01-12 | 2005-02-22 | Method and stimulating oil and gas wells using deformable proppants |
CA2715597A Active CA2715597C (en) | 2005-01-12 | 2005-02-22 | Method of stimulating oil and gas wells using deformable proppants |
Family Applications After (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CA2715597A Active CA2715597C (en) | 2005-01-12 | 2005-02-22 | Method of stimulating oil and gas wells using deformable proppants |
Country Status (2)
Country | Link |
---|---|
US (3) | US7322411B2 (en) |
CA (2) | CA2497948C (en) |
Families Citing this family (99)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US7322411B2 (en) * | 2005-01-12 | 2008-01-29 | Bj Services Company | Method of stimulating oil and gas wells using deformable proppants |
US8012533B2 (en) | 2005-02-04 | 2011-09-06 | Oxane Materials, Inc. | Composition and method for making a proppant |
US7867613B2 (en) | 2005-02-04 | 2011-01-11 | Oxane Materials, Inc. | Composition and method for making a proppant |
ATE531895T1 (en) | 2005-02-04 | 2011-11-15 | Oxane Materials Inc | COMPOSITION AND METHOD FOR PRODUCING A SUPPORTANT |
US7491444B2 (en) | 2005-02-04 | 2009-02-17 | Oxane Materials, Inc. | Composition and method for making a proppant |
US7528096B2 (en) * | 2005-05-12 | 2009-05-05 | Bj Services Company | Structured composite compositions for treatment of subterranean wells |
DE102005045180B4 (en) | 2005-09-21 | 2007-11-15 | Center For Abrasives And Refractories Research & Development C.A.R.R.D. Gmbh | Spherical corundum grains based on molten aluminum oxide and a process for their preparation |
US7836952B2 (en) * | 2005-12-08 | 2010-11-23 | Halliburton Energy Services, Inc. | Proppant for use in a subterranean formation |
CA2536957C (en) * | 2006-02-17 | 2008-01-22 | Jade Oilfield Service Ltd. | Method of treating a formation using deformable proppants |
US7931087B2 (en) * | 2006-03-08 | 2011-04-26 | Baker Hughes Incorporated | Method of fracturing using lightweight polyamide particulates |
US8562900B2 (en) | 2006-09-01 | 2013-10-22 | Imerys | Method of manufacturing and using rod-shaped proppants and anti-flowback additives |
FR2910368B1 (en) * | 2006-12-22 | 2012-03-09 | Rhodia Operations | POLYAMIDE PEARLS AND PROCESS FOR THE PRODUCTION THEREOF |
RU2006147204A (en) * | 2006-12-29 | 2008-07-10 | Шлюмбергер Текнолоджи Б.В. (Nl) | METHOD FOR PREVENTING THE PROPANTA |
WO2008092078A1 (en) * | 2007-01-26 | 2008-07-31 | Bj Services Company | Fracture acidizing method utilizing reactive fluids and deformable particulates |
RU2351632C2 (en) * | 2007-03-22 | 2009-04-10 | Шлюмбергер Текнолоджи Б.В. | Proppant and method of proppant producing |
US20090029878A1 (en) * | 2007-07-24 | 2009-01-29 | Jozef Bicerano | Drilling fluid, drill-in fluid, completition fluid, and workover fluid additive compositions containing thermoset nanocomposite particles; and applications for fluid loss control and wellbore strengthening |
US8276664B2 (en) * | 2007-08-13 | 2012-10-02 | Baker Hughes Incorporated | Well treatment operations using spherical cellulosic particulates |
CN101903453B (en) * | 2007-12-14 | 2013-11-06 | 普拉德研究及开发股份有限公司 | Proppants and uses thereof |
US7950455B2 (en) * | 2008-01-14 | 2011-05-31 | Baker Hughes Incorporated | Non-spherical well treating particulates and methods of using the same |
US8198219B2 (en) | 2008-02-22 | 2012-06-12 | Basf Se | Method for producing solid materials on the basis of synthetic polymers and/or biopolymers and use thereof |
US7814980B2 (en) * | 2008-04-10 | 2010-10-19 | Halliburton Energy Services, Inc. | Micro-crosslinked gels and associated methods |
US8006760B2 (en) * | 2008-04-10 | 2011-08-30 | Halliburton Energy Services, Inc. | Clean fluid systems for partial monolayer fracturing |
US8012582B2 (en) * | 2008-09-25 | 2011-09-06 | Halliburton Energy Services, Inc. | Sintered proppant made with a raw material containing alkaline earth equivalent |
US8205675B2 (en) | 2008-10-09 | 2012-06-26 | Baker Hughes Incorporated | Method of enhancing fracture conductivity |
EP2192094A1 (en) * | 2008-11-27 | 2010-06-02 | Services Pétroliers Schlumberger | Aqueous resin compositions and methods for cement repair |
US7896078B2 (en) * | 2009-01-14 | 2011-03-01 | Baker Hughes Incorporated | Method of using crosslinkable brine containing compositions |
CN101880524A (en) | 2010-04-27 | 2010-11-10 | 福建省宁德市俊杰瓷业有限公司 | Ultra-low-density ceramic proppant and preparation method thereof |
US9845427B2 (en) * | 2009-10-20 | 2017-12-19 | Self-Suspending Proppant Llc | Proppants for hydraulic fracturing technologies |
MX2012007248A (en) | 2009-12-22 | 2012-07-30 | Oxane Materials Inc | A proppant having a glass-ceramic material. |
US20110259588A1 (en) * | 2010-04-21 | 2011-10-27 | Ali Syed A | Methods of stabilizing shale surface to minimize proppant embedment and increase proppant-pack conductivity |
CA2806573A1 (en) | 2010-07-29 | 2012-02-02 | 3M Innovative Properties Company | Elastomer-modified crosslinked epoxy vinyl ester particles and methods for making and using the same |
US8517095B2 (en) | 2010-08-09 | 2013-08-27 | Baker Hughes Incorporated | Method of using hexose oxidases to create hydrogen peroxide in aqueous well treatment fluids |
US9290690B2 (en) | 2011-05-03 | 2016-03-22 | Preferred Technology, Llc | Coated and cured proppants |
US9040467B2 (en) | 2011-05-03 | 2015-05-26 | Preferred Technology, Llc | Coated and cured proppants |
US8763700B2 (en) | 2011-09-02 | 2014-07-01 | Robert Ray McDaniel | Dual function proppants |
US9725645B2 (en) | 2011-05-03 | 2017-08-08 | Preferred Technology, Llc | Proppant with composite coating |
US8993489B2 (en) | 2011-05-03 | 2015-03-31 | Preferred Technology, Llc | Coated and cured proppants |
US20130025867A1 (en) | 2011-07-29 | 2013-01-31 | Mary Michele Stevens | Method of slickwater fracturing |
US9297244B2 (en) | 2011-08-31 | 2016-03-29 | Self-Suspending Proppant Llc | Self-suspending proppants for hydraulic fracturing comprising a coating of hydrogel-forming polymer |
CA2845840C (en) | 2011-08-31 | 2020-02-25 | Self-Suspending Proppant Llc | Self-suspending proppants for hydraulic fracturing |
US20140000891A1 (en) | 2012-06-21 | 2014-01-02 | Self-Suspending Proppant Llc | Self-suspending proppants for hydraulic fracturing |
US9868896B2 (en) | 2011-08-31 | 2018-01-16 | Self-Suspending Proppant Llc | Self-suspending proppants for hydraulic fracturing |
CN102329607A (en) * | 2011-10-26 | 2012-01-25 | 西安荣翔精细化工有限责任公司 | Low-density organic proppant |
US8899332B2 (en) | 2011-11-22 | 2014-12-02 | Baker Hughes Incorporated | Method for building and forming a plug in a horizontal wellbore |
US9637675B2 (en) | 2011-11-22 | 2017-05-02 | Baker Hughes Incorporated | Use of composites having deformable core and viscosifying agent coated thereon in well treatment operations |
US9580642B2 (en) | 2011-11-22 | 2017-02-28 | Baker Hughes Incorporated | Method for improving isolation of flow to completed perforated intervals |
CA2858545A1 (en) * | 2011-12-06 | 2013-06-13 | Imerys Oilfield Minerals, Inc. | Granulated inorganic particulates and their use in oilfield applications |
NL1039259C2 (en) | 2011-12-22 | 2013-07-01 | Joa Technology Beheer B V | Method for the preparation of polymer comprising particles. |
NL1039260C2 (en) | 2011-12-22 | 2013-06-26 | Resin Proppants Internat B V | Method for the preparation of polymer comprising particles. |
US9562187B2 (en) | 2012-01-23 | 2017-02-07 | Preferred Technology, Llc | Manufacture of polymer coated proppants |
US20130203637A1 (en) | 2012-02-02 | 2013-08-08 | D. V. Satyanarayana Gupta | Method of delaying crosslinking in well treatment operation |
RU2622573C2 (en) | 2012-02-06 | 2017-06-16 | Бэйкер Хьюз Инкорпорейтед | Way of hydraulic seam fracture by means of ultra low mass proppant suspended mixtures and gas streams |
US9896918B2 (en) | 2012-07-27 | 2018-02-20 | Mbl Water Partners, Llc | Use of ionized water in hydraulic fracturing |
US8424784B1 (en) | 2012-07-27 | 2013-04-23 | MBJ Water Partners | Fracture water treatment method and system |
US9540561B2 (en) * | 2012-08-29 | 2017-01-10 | Halliburton Energy Services, Inc. | Methods for forming highly conductive propped fractures |
US9803131B2 (en) | 2012-11-02 | 2017-10-31 | Wacker Chemical Corporation | Oil and gas well proppants of silicone-resin-modified phenolic resins |
US9429006B2 (en) | 2013-03-01 | 2016-08-30 | Baker Hughes Incorporated | Method of enhancing fracture conductivity |
US10221660B2 (en) | 2013-03-15 | 2019-03-05 | Melior Innovations, Inc. | Offshore methods of hydraulically fracturing and recovering hydrocarbons |
US9499677B2 (en) | 2013-03-15 | 2016-11-22 | Melior Innovations, Inc. | Black ceramic additives, pigments, and formulations |
US9518214B2 (en) | 2013-03-15 | 2016-12-13 | Preferred Technology, Llc | Proppant with polyurea-type coating |
US9815952B2 (en) | 2013-03-15 | 2017-11-14 | Melior Innovations, Inc. | Solvent free solid material |
US10167366B2 (en) | 2013-03-15 | 2019-01-01 | Melior Innovations, Inc. | Polysilocarb materials, methods and uses |
US9815943B2 (en) | 2013-03-15 | 2017-11-14 | Melior Innovations, Inc. | Polysilocarb materials and methods |
CA2910822A1 (en) * | 2013-05-02 | 2014-11-06 | Melior Technology, Inc. | Polysilocarb materials and methods |
US10322936B2 (en) | 2013-05-02 | 2019-06-18 | Pallidus, Inc. | High purity polysilocarb materials, applications and processes |
US9481781B2 (en) | 2013-05-02 | 2016-11-01 | Melior Innovations, Inc. | Black ceramic additives, pigments, and formulations |
US9919972B2 (en) | 2013-05-02 | 2018-03-20 | Melior Innovations, Inc. | Pressed and self sintered polymer derived SiC materials, applications and devices |
US11014819B2 (en) | 2013-05-02 | 2021-05-25 | Pallidus, Inc. | Methods of providing high purity SiOC and SiC materials |
US11091370B2 (en) | 2013-05-02 | 2021-08-17 | Pallidus, Inc. | Polysilocarb based silicon carbide materials, applications and devices |
US9657409B2 (en) | 2013-05-02 | 2017-05-23 | Melior Innovations, Inc. | High purity SiOC and SiC, methods compositions and applications |
US10100247B2 (en) | 2013-05-17 | 2018-10-16 | Preferred Technology, Llc | Proppant with enhanced interparticle bonding |
CN105745299B (en) * | 2013-07-04 | 2020-03-13 | 美利尔创新公司 | High strength low density synthetic proppant for hydraulic fracturing and recovery of hydrocarbons |
US10308868B2 (en) * | 2014-01-02 | 2019-06-04 | Halliburton Energy Services, Inc. | Generating and enhancing microfracture conductivity |
US9932521B2 (en) | 2014-03-05 | 2018-04-03 | Self-Suspending Proppant, Llc | Calcium ion tolerant self-suspending proppants |
US9790422B2 (en) | 2014-04-30 | 2017-10-17 | Preferred Technology, Llc | Proppant mixtures |
CN104046134B (en) * | 2014-06-29 | 2016-05-18 | 桂林理工大学 | A kind of method of making micronic dust chalk of peach gum |
EP3186331B1 (en) | 2014-07-23 | 2022-05-04 | Baker Hughes Holdings LLC | Composite comprising well treatment agent and/or a tracer adhered onto a calcined substrate of a metal oxide coated core and a method of using the same |
US20160201441A1 (en) * | 2015-01-08 | 2016-07-14 | Schlumberger Technology Corporation | Selection of propping agent for heterogeneous proppant placement applications |
EP3061800A1 (en) * | 2015-02-26 | 2016-08-31 | Repsol, S.A. | Ultra-high-molecular-weight polyolefin proppants |
US10253250B2 (en) * | 2015-04-28 | 2019-04-09 | Halliburton Energy Services, Inc. | Forming conductive arch channels in subterranean formation fractures |
US9862881B2 (en) | 2015-05-13 | 2018-01-09 | Preferred Technology, Llc | Hydrophobic coating of particulates for enhanced well productivity |
US10590337B2 (en) | 2015-05-13 | 2020-03-17 | Preferred Technology, Llc | High performance proppants |
CN105550410B (en) * | 2015-12-07 | 2018-08-31 | 西南石油大学 | The method for calculating shale reservoir hydraulic fracturing dipping fracture induced stress |
CN105550780B (en) * | 2015-12-28 | 2020-03-10 | 中国石油天然气股份有限公司 | Method and device for predicting cold damage of fracturing fluid to capacity of compact oil |
CN105973667A (en) * | 2016-05-09 | 2016-09-28 | 贵州大学 | Preparation method of sample for hydraulic fracturing experiment of shale |
US11041111B2 (en) * | 2016-06-23 | 2021-06-22 | Halliburton Energy Services, Inc. | Enhanced propped fracture conductivity in subterranean wells |
CA3024784C (en) | 2016-06-23 | 2021-06-08 | Halliburton Energy Services, Inc. | Proppant-free channels in a propped fracture using ultra-low density, degradable particulates |
US11208591B2 (en) | 2016-11-16 | 2021-12-28 | Preferred Technology, Llc | Hydrophobic coating of particulates for enhanced well productivity |
US10696896B2 (en) | 2016-11-28 | 2020-06-30 | Prefferred Technology, Llc | Durable coatings and uses thereof |
US10385261B2 (en) | 2017-08-22 | 2019-08-20 | Covestro Llc | Coated particles, methods for their manufacture and for their use as proppants |
US20200048532A1 (en) | 2018-08-10 | 2020-02-13 | Bj Services, Llc | Frac Fluids for Far Field Diversion |
US10752829B2 (en) | 2018-10-25 | 2020-08-25 | Cnpc Usa Corporation | Compositions of hydraulic fracturing fluid and method thereof |
WO2020106655A1 (en) | 2018-11-21 | 2020-05-28 | Self-Suspending Proppant Llc | Salt-tolerant self-suspending proppants made without extrusion |
CN109575248B (en) * | 2018-11-28 | 2021-09-28 | 中国石油集团渤海钻探工程有限公司 | Controllable degradable terpolymer temporary plugging agent, preparation method and use method |
CN109517593A (en) * | 2018-11-29 | 2019-03-26 | 江苏华普泰克石油装备有限公司 | A kind of preparation method of ceramsite sand |
WO2020185373A1 (en) | 2019-03-11 | 2020-09-17 | Dow Global Technologies Llc | Coated proppants |
CN110306964B (en) * | 2019-07-02 | 2020-08-21 | 中国矿业大学 | Hydraulic fracturing coal seam crack visualization and permeability increasing effect evaluation method |
US11447685B2 (en) | 2019-08-28 | 2022-09-20 | Halliburton Energy Services, Inc. | Methods of stabilizing carbonate-bearing formations |
US11396625B2 (en) | 2019-09-17 | 2022-07-26 | Saudi Arabian Oil Company | Coated proppant and methods of making and use thereof |
Family Cites Families (56)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3089542A (en) * | 1960-04-13 | 1963-05-14 | American Cyanamid Co | Oil well fracturing method |
US3149674A (en) * | 1961-08-23 | 1964-09-22 | Jersey Prod Res Co | Fracturing of subsurface earth formations |
US3149673A (en) * | 1961-08-23 | 1964-09-22 | Jersey Prod Res Co | Use of solid polyolefin propping agent in hydraulic fracturing |
US3175615A (en) * | 1962-10-29 | 1965-03-30 | Jersey Prod Res Co | Fracturing of subsurface earth formations |
US3254717A (en) * | 1962-11-19 | 1966-06-07 | Gulf Research Development Co | Fracturing process and impregnated propping agent for use therein |
US3266573A (en) * | 1964-03-25 | 1966-08-16 | Pan American Petroleum Corp | Method of fracturing subsurface formations |
US3481401A (en) * | 1968-01-25 | 1969-12-02 | Exxon Production Research Co | Self-bridging fractures |
DE1918600B1 (en) | 1969-04-12 | 1970-12-10 | Gehlen Dipl Ing Dr Rer Pol Her | Vehicle with a removable ramp for building bridges, especially swimming bridges, and ferries |
US3659651A (en) | 1970-08-17 | 1972-05-02 | Exxon Production Research Co | Hydraulic fracturing using reinforced resin pellets |
US3888311A (en) * | 1973-10-01 | 1975-06-10 | Exxon Production Research Co | Hydraulic fracturing method |
US3933205A (en) | 1973-10-09 | 1976-01-20 | Othar Meade Kiel | Hydraulic fracturing process using reverse flow |
US3998744A (en) | 1975-04-16 | 1976-12-21 | Standard Oil Company | Oil fracturing spacing agents |
US4547468A (en) | 1981-08-10 | 1985-10-15 | Terra Tek, Inc. | Hollow proppants and a process for their manufacture |
US4553596A (en) | 1982-10-27 | 1985-11-19 | Santrol Products, Inc. | Well completion technique |
GB8317228D0 (en) | 1983-06-24 | 1983-07-27 | Exxon Research Engineering Co | Magnetizable adsorbents |
US4527627A (en) | 1983-07-28 | 1985-07-09 | Santrol Products, Inc. | Method of acidizing propped fractures |
US4512405A (en) | 1984-02-29 | 1985-04-23 | Hughes Tool Company | Pneumatic transfer of solids into wells |
US5305832A (en) | 1992-12-21 | 1994-04-26 | The Western Company Of North America | Method for fracturing high temperature subterranean formations |
US5422183A (en) | 1993-06-01 | 1995-06-06 | Santrol, Inc. | Composite and reinforced coatings on proppants and particles |
US5837656A (en) | 1994-07-21 | 1998-11-17 | Santrol, Inc. | Well treatment fluid compatible self-consolidating particles |
US5929002A (en) | 1994-07-28 | 1999-07-27 | Dowell, A Division Of Schlumberger Technology Corporation | Fluid loss control |
US5531274A (en) | 1994-07-29 | 1996-07-02 | Bienvenu, Jr.; Raymond L. | Lightweight proppants and their use in hydraulic fracturing |
US5562160A (en) | 1994-08-08 | 1996-10-08 | B. J. Services Company | Fracturing fluid treatment design to optimize fluid rheology and proppant pack conductivity |
US20050028979A1 (en) | 1996-11-27 | 2005-02-10 | Brannon Harold Dean | Methods and compositions of a storable relatively lightweight proppant slurry for hydraulic fracturing and gravel packing applications |
US7426961B2 (en) | 2002-09-03 | 2008-09-23 | Bj Services Company | Method of treating subterranean formations with porous particulate materials |
US6772838B2 (en) | 1996-11-27 | 2004-08-10 | Bj Services Company | Lightweight particulate materials and uses therefor |
US6364018B1 (en) | 1996-11-27 | 2002-04-02 | Bj Services Company | Lightweight methods and compositions for well treating |
US6749025B1 (en) | 1996-11-27 | 2004-06-15 | Bj Services Company | Lightweight methods and compositions for sand control |
US6330916B1 (en) | 1996-11-27 | 2001-12-18 | Bj Services Company | Formation treatment method using deformable particles |
US6059034A (en) | 1996-11-27 | 2000-05-09 | Bj Services Company | Formation treatment method using deformable particles |
CA2291245C (en) * | 1997-05-27 | 2008-11-25 | Bj Services Company | Improved polymer expansion for oil and gas recovery |
US6169058B1 (en) | 1997-06-05 | 2001-01-02 | Bj Services Company | Compositions and methods for hydraulic fracturing |
US5908073A (en) | 1997-06-26 | 1999-06-01 | Halliburton Energy Services, Inc. | Preventing well fracture proppant flow-back |
US6451953B1 (en) | 1997-12-18 | 2002-09-17 | Sun Drilling Products, Corp. | Chain entanglement crosslinked polymers |
AR019461A1 (en) | 1998-07-22 | 2002-02-20 | Borden Chem Inc | A COMPOSITE PARTICLE, A METHOD TO PRODUCE, A METHOD TO TREAT A HYDRAULICALLY INDUCED FRACTURE IN A UNDERGROUND FORMATION, AND A METHOD FOR WATER FILTRATION. |
US6406789B1 (en) | 1998-07-22 | 2002-06-18 | Borden Chemical, Inc. | Composite proppant, composite filtration media and methods for making and using same |
US6017655A (en) | 1998-08-18 | 2000-01-25 | Ovonic Battery Company | Nickel hydroxide positive electrode material exhibiting improved conductivity and engineered activation energy |
CA2318703A1 (en) | 1999-09-16 | 2001-03-16 | Bj Services Company | Compositions and methods for cementing using elastic particles |
US6279656B1 (en) | 1999-11-03 | 2001-08-28 | Santrol, Inc. | Downhole chemical delivery system for oil and gas wells |
US6779604B2 (en) | 2000-06-05 | 2004-08-24 | Exxonmobil Upstream Research Company | Deformable gravel pack and method of forming |
US6439309B1 (en) | 2000-12-13 | 2002-08-27 | Bj Services Company | Compositions and methods for controlling particulate movement in wellbores and subterranean formations |
US6562160B2 (en) * | 2001-04-10 | 2003-05-13 | The United States Of America As Represented By The Secretary Of The Navy | Airbag propellant |
US7153575B2 (en) * | 2002-06-03 | 2006-12-26 | Borden Chemical, Inc. | Particulate material having multiple curable coatings and methods for making and using same |
US6732800B2 (en) * | 2002-06-12 | 2004-05-11 | Schlumberger Technology Corporation | Method of completing a well in an unconsolidated formation |
US6742590B1 (en) | 2002-09-05 | 2004-06-01 | Halliburton Energy Services, Inc. | Methods of treating subterranean formations using solid particles and other larger solid materials |
US6832650B2 (en) | 2002-09-11 | 2004-12-21 | Halliburton Energy Services, Inc. | Methods of reducing or preventing particulate flow-back in wells |
WO2004083600A1 (en) | 2003-03-18 | 2004-09-30 | Bj Services Company | Method of treating subterranean formations using mixed density proppants or sequential proppant stages |
CN1839034A (en) * | 2003-04-15 | 2006-09-27 | 氦克逊特种化学品公司 | Particulate material containing thermoplastic elastomer and methods for making and using same |
US7207386B2 (en) | 2003-06-20 | 2007-04-24 | Bj Services Company | Method of hydraulic fracturing to reduce unwanted water production |
US7213651B2 (en) | 2004-06-10 | 2007-05-08 | Bj Services Company | Methods and compositions for introducing conductive channels into a hydraulic fracturing treatment |
US20060047027A1 (en) | 2004-08-24 | 2006-03-02 | Brannon Harold D | Well treatment fluids containing a multimodal polymer system |
US7255169B2 (en) | 2004-09-09 | 2007-08-14 | Halliburton Energy Services, Inc. | Methods of creating high porosity propped fractures |
US7281580B2 (en) | 2004-09-09 | 2007-10-16 | Halliburton Energy Services, Inc. | High porosity fractures and methods of creating high porosity fractures |
US20060073980A1 (en) | 2004-09-30 | 2006-04-06 | Bj Services Company | Well treating composition containing relatively lightweight proppant and acid |
US7726399B2 (en) | 2004-09-30 | 2010-06-01 | Bj Services Company | Method of enhancing hydraulic fracturing using ultra lightweight proppants |
US7322411B2 (en) * | 2005-01-12 | 2008-01-29 | Bj Services Company | Method of stimulating oil and gas wells using deformable proppants |
-
2005
- 2005-01-12 US US11/034,388 patent/US7322411B2/en active Active
- 2005-02-22 CA CA2497948A patent/CA2497948C/en active Active
- 2005-02-22 CA CA2715597A patent/CA2715597C/en active Active
-
2008
- 2008-01-28 US US12/021,089 patent/US7789147B2/en active Active
-
2010
- 2010-09-03 US US12/875,730 patent/US20110000667A1/en not_active Abandoned
Also Published As
Publication number | Publication date |
---|---|
US7789147B2 (en) | 2010-09-07 |
CA2715597C (en) | 2014-12-02 |
US20080110623A1 (en) | 2008-05-15 |
US20060151170A1 (en) | 2006-07-13 |
CA2715597A1 (en) | 2006-07-12 |
CA2497948A1 (en) | 2006-07-12 |
US20110000667A1 (en) | 2011-01-06 |
US7322411B2 (en) | 2008-01-29 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CA2497948C (en) | Method and stimulating oil and gas wells using deformable proppants | |
US7726399B2 (en) | Method of enhancing hydraulic fracturing using ultra lightweight proppants | |
US7772163B1 (en) | Well treating composite containing organic lightweight material and weight modifying agent | |
US20060073980A1 (en) | Well treating composition containing relatively lightweight proppant and acid | |
US6330916B1 (en) | Formation treatment method using deformable particles | |
US7207386B2 (en) | Method of hydraulic fracturing to reduce unwanted water production | |
US10087364B2 (en) | Method of stimulating a subterranean formation with non-spherical ceramic proppants | |
US7931087B2 (en) | Method of fracturing using lightweight polyamide particulates | |
US6059034A (en) | Formation treatment method using deformable particles | |
CA2644213C (en) | Method of treating subterranean formations using mixed density proppants or sequential proppant stages | |
US8122957B2 (en) | Sand control method using porous particulate materials | |
US8393394B2 (en) | Methods for strengthening fractures in subterranean formations | |
WO1999027229A1 (en) | Formation treatment method using deformable particles | |
RU2687722C2 (en) | Reinforced proppant clusters for formation hydraulic fracturing | |
GB2319796A (en) | Formation treatment method using deformable particles | |
NO342605B1 (en) | Proppant or sand control particulate material of a selectively configured porous material and method of treating underground formations with this material | |
WO2001066908A2 (en) | Lightweight compositions and methods for sand control | |
US3239006A (en) | Mixed props for high flow capacity fractures | |
GB2359316A (en) | A composition and method for fracturing a subterranean formation | |
GB2399118A (en) | Fracture proppant with particles having a deformable core and a deformable coating |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
EEER | Examination request |