In the drilling and completion industry, the formation of boreholes for the purpose of production or injection of fluids is common. The boreholes are used for exploration or extraction of natural resources such as hydrocarbons, oil, gas, water, and CO2 sequestration. For enhancing production and increasing extraction rates from a subterranean borehole, the formation walls of the borehole may be fractured using a pressurized slurry, proppant containing fracturing fluid, or other treating fluids. The fractures in the formation wall may be held open with the particulates once the injection of fracturing fluids has ceased.
A conventional fracturing system passes pressurized fracturing fluid through a tubular string that extends downhole through the borehole that traverses the zones to be fractured. The string may include valves that are opened to allow for the fracturing fluid to be directed towards a targeted zone. To remotely open the valves from the surface, a ball is dropped into the string and lands on a ball seat associated with a particular valve to block fluid flow through the string and consequently build up pressure uphole of the ball which forces a sleeve downhole thus opening a port in the wall of the string. When multiple zones are involved, the ball seats are of varying sizes with a downhole most seat being the smallest and an uphole most seat being the largest, such that balls of increasing diameter are sequentially dropped into the string to sequentially open the valves from the downhole end to an uphole end. Thus, the zones of the borehole are fractured in a “bottom-up” approach by starting with fracturing a downhole-most zone and working upwards towards an uphole-most zone.
To avoid the inevitable complications associated with employing differently sized ball seats, the smallest of which may overly restrict the flow through the string, and correspondingly different sized balls, the use of deformable balls and ball seats has been proposed, however the rate at which the balls are forced through the ball seats introduces additional complexities including dealing with different rates of deformation of the selected material since it may not function as desired in downhole environments. Also, despite providing certain advantages over using differently sized balls, the order of fracturing operations is still limited to the “bottom-up” approach.
A selective downhole tool includes a tubular having a longitudinal bore enabling passage of fluids there through and having a valve opening in a wall of the tubular; an expandable ball seat selectively movable between a first size sized to trap a ball to block flow through the tubular and a larger second size sized to release the ball through the tubular; and a valve cover longitudinally movable within the tubular, the valve cover including a dissolvable insert.
A method of operating a downhole tool, the method includes running the downhole tool in a bore hole, the tool including a tubular having a valve opening covered by a valve cover; moving the valve cover longitudinally to expose the valve opening; recovering the valve opening with the valve cover subsequent an operation through the valve opening; and dissolving a portion of the valve cover to re-expose the valve opening.
The following descriptions should not be considered limiting in any way. With reference to the accompanying drawings, like elements are numbered alike:
A detailed description of one or more embodiments of the disclosed apparatus and method are presented herein by way of exemplification and not limitation with reference to the Figures.
A selective hydraulic fracturing tool 100, shown in
An exemplary embodiment of the selective hydraulic fracturing tool 100 is shown in
The tool includes an expandable ball seat 150 that allows an operator to use a single sized ball for all zones, and thus provides for a mono-bore operation that allows both improved simplicity in manufacturing the tool 100 as well as improved simplicity in operation. While a spherical ball is typically employed in such an operation, the term ball includes any shaped object which can be dropped into the bore 108 and be trapped and subsequently released from the ball seat 150. A j-mechanism indexing apparatus 200 provides alternate positions for the ball seat 150 to be located in and allows balls to pass through the ball seat 150 without shearing/activating the tool 100. A valve cover 250 includes dissolvable material that allows an insert 252 to close off a fractured zone and then dissolve, without intervention, to allow production from the zone after the borehole 10 is completed.
In an exemplary embodiment of the expandable ball seat 150, a collet 152 including a plurality of fingers 154 is engaged with the indexing apparatus 200. The ball seat 150 is shown by itself in
While a collet 152 has been described for forming the expandable ball seat 150, an alternative exemplary embodiment of an expandable ball seat may include a split ring or “C” ring where movement of the indexing apparatus 200, or a feature connected to the indexing apparatus 200, between the body 106 and the ring will force the ring to be compressed to thereby reduce an inner diameter of the ring thus preventing a ball 50 from passing there through until movement of the indexing apparatus 200 away from the ring opens the ring to increase the aperture size of the ring allowing for passage of the ball 50.
In an exemplary embodiment of the j-mechanism indexing apparatus 200, the apparatus 200 includes an indexing sleeve 202 having a central longitudinal aperture 204 for fluid flow, where the aperture 204 passes through the bore 108 of the tubular body 106. The sleeve 202 also includes an indexing path 206, such as a groove, that is formed about a diameter of the sleeve 202. A portion of the indexing path 206 is shown in
The outer middle body portion 110 of the tool 100 is connected to a downhole body portion 112 of the tool 100. The downhole body portion 112 of the tool 100 includes an indented section 114 that includes an uphole surface 116 that contacts a downhole end 224 of the compression spring 218. The indented section 114 of the downhole body portion 112 is attached to a downhole end 118 of the middle body portion 110, where the middle body portion is indented to match and overlap the indented section 114 of the downhole body portion 112. A downhole end 262 of the valve sleeve 254 is fixedly attached to the movable tubular section 216 and therefore surrounds the spring member 220, ball seat 150, and inner tubular 172. An uphole body portion 120 of the tool 100 surrounds an uphole portion of the valve sleeve 254. The downhole end 122 of the uphole body portion 120 is connected to the outer middle body portion 110. The uphole body portion 120 includes a valve opening 124 for allowing a fracturing operation to occur by allowing the passage of fracturing fluids there through. The valve opening 124 may also be used for the passage of production fluids or other downhole operations. The uphole body portion 120 is connected to the valve sleeve 254 by a shear pin 126.
In an exemplary embodiment of the valve cover 250, the valve cover 250 includes the valve sleeve 254 as previously described as connected via a shear pin 126 to the uphole body portion 120 and connected to the movable tubular section 216 at the downhole end 262 of the valve sleeve 254. An indent 264 for a seal 266 is provided at an uphole end 268 of the valve sleeve 254, and an indent 270 for a seal 272 is provided at a central area of the valve sleeve 254. The valve cover 250 also includes the dissolvable insert 252 made of a dissolvable material, and the insert 252 is located downhole of the seal 266 provided at the uphole end 268 of the valve sleeve 254. In a run-in position, as shown in
United States Patent Publication No. 2011/0135953 (Xu, et al.) is hereby incorporated by reference in its entirety. The dissolvable material of the insert 252 may include a controlled electrolytic metallic material 300, as shown in
The materials 300 in the dissolvable inserts 252 as described herein are lightweight, high-strength metallic materials. These lightweight, high-strength and selectably and controllably degradable materials 300 include fully-dense, sintered powder compacts formed from coated powder materials that include various lightweight particle cores and core materials having various single layer and multilayer nanoscale coatings. These powder compacts are made from coated metallic powders that include various electrochemically-active (e.g., having relatively higher standard oxidation potentials) lightweight, high-strength particle cores and core materials, such as electrochemically active metals, that are dispersed within a cellular nanomatrix formed from the various nanoscale metallic coating layers of metallic coating materials, and are particularly useful in borehole applications. These powder compacts provide a unique and advantageous combination of mechanical strength properties, such as compression and shear strength, low density and selectable and controllable corrosion properties, particularly rapid and controlled dissolution in various borehole fluids. For example, the particle core and coating layers of these powders may be selected to provide sintered powder compacts suitable for use as high strength engineered materials having a compressive strength and shear strength comparable to various other engineered materials, including carbon, stainless and alloy steels, but which also have a low density comparable to various polymers, elastomers, low-density porous ceramics and composite materials. As yet another example, these powders and powder compact materials may be configured to provide a selectable and controllable degradation or disposal in response to a change in an environmental condition, such as a transition from a very low dissolution rate to a very rapid dissolution rate in response to a change in a property or condition of a borehole proximate the dissolvable inserts 252 formed from the compact, including a property change in a borehole fluid that is in contact with the powder compact. The selectable and controllable degradation or disposal characteristics described also allow the dimensional stability and strength of the dissolvable inserts 252 made from these materials to be maintained until they are no longer needed, at which time a predetermined environmental condition, such as a borehole condition, including borehole fluid temperature, pressure or pH value, may be changed to promote their removal by rapid dissolution. These coated powder materials and powder compacts and engineered materials formed from them, as well as methods of making them, are described further below.
Referring to
Each of the metallic, coated powder particles 312 of powder 310 includes a particle core 314 and a metallic coating layer 316 disposed on the particle core 314. The particle core 314 includes a core material 318. The core material 318 may include any suitable material for forming the particle core 314 that provides powder particle 312 that can be sintered to form a lightweight, high-strength powder compact 400 having selectable and controllable dissolution characteristics. Suitable core materials include electrochemically active metals having a standard oxidation potential greater than or equal to that of Zn, including as Mg, Al, Mn or Zn or a combination thereof. These electrochemically active metals are very reactive with a number of common borehole fluids, including any number of ionic fluids or highly polar fluids, such as those that contain various chlorides. Examples include fluids comprising potassium chloride (KCl), hydrochloric acid (HCl), calcium chloride (CaCl2), calcium bromide (CaBr2) or zinc bromide (ZnBr2). Core material 318 may also include other metals that are less electrochemically active than Zn or non-metallic materials, or a combination thereof. Suitable non-metallic materials include ceramics, composites, glasses or carbon, or a combination thereof. Core material 318 may be selected to provide a high dissolution rate in a predetermined borehole fluid, but may also be selected to provide a relatively low dissolution rate, including zero dissolution, where dissolution of the nanomatrix material causes the particle core 314 to be rapidly undermined and liberated from the particle compact at the interface with the borehole fluid, such that the effective rate of dissolution of particle compacts made using particle cores 314 of these core materials 318 is high, even though core material 318 itself may have a low dissolution rate, including core materials 318 that may be substantially insoluble in the borehole fluid.
With regard to the electrochemically active metals as core materials 318, including Mg, Al, Mn or Zn, these metals may be used as pure metals or in any combination with one another, including various alloy combinations of these materials, including binary, tertiary, or quaternary alloys of these materials. These combinations may also include composites of these materials. Further, in addition to combinations with one another, the Mg, Al, Mn or Zn core materials 318 may also include other constituents, including various alloying additions, to alter one or more properties of the particle cores 314, such as by improving the strength, lowering the density or altering the dissolution characteristics of the core material 318.
Among the electrochemically active metals, Mg, either as a pure metal or an alloy or a composite material, is particularly useful, because of its low density and ability to form high-strength alloys, as well as its high degree of electrochemical activity, since it has a standard oxidation potential higher than Al, Mn or Zn. Mg alloys include all alloys that have Mg as an alloy constituent. Mg alloys that combine other electrochemically active metals, as described herein, as alloy constituents are particularly useful, including binary Mg—Zn, Mg—Al and Mg—Mn alloys, as well as tertiary Mg—Zn—Y and Mg—Al—X alloys, where X includes Zn, Mn, Si, Ca or Y, or a combination thereof. These Mg—Al—X alloys may include, by weight, up to about 85% Mg, up to about 15% Al and up to about 5% X. Particle core 314 and core material 318, and particularly electrochemically active metals including Mg, Al, Mn or Zn, or combinations thereof, may also include a rare earth element or combination of rare earth elements. As used herein, rare earth elements include Sc, Y, La, Ce, Pr, Nd or Er, or a combination of rare earth elements. Where present, a rare earth element or combinations of rare earth elements may be present, by weight, in an amount of about 5% or less.
Particle core 314 and core material 318 have a melting temperature (TP). As used herein, TP includes the lowest temperature at which incipient melting or liquation or other forms of partial melting occur within core material 318, regardless of whether core material 318 comprises a pure metal, an alloy with multiple phases having different melting temperatures or a composite of materials having different melting temperatures.
Particle cores 314 may have any suitable particle size or range of particle sizes or distribution of particle sizes. For example, the particle cores 314 may be selected to provide an average particle size that is represented by a normal or Gaussian type unimodal distribution around an average or mean, as illustrated generally in
Particle cores 314 may have any suitable particle shape, including any regular or irregular geometric shape, or combination thereof. In an exemplary embodiment, particle cores 314 are substantially spheroidal electrochemically active metal particles. In another exemplary embodiment, particle cores 314 are substantially irregularly shaped ceramic particles. In yet another exemplary embodiment, particle cores 314 are carbon or other nanotube structures or hollow glass microspheres.
Each of the metallic, coated powder particles 312 of powder 310 also includes a metallic coating layer 316 that is disposed on particle core 314. Metallic coating layer 316 includes a metallic coating material 320. Metallic coating material 320 gives the powder particles 312 and powder 310 its metallic nature. Metallic coating layer 316 is a nanoscale coating layer. In an exemplary embodiment, metallic coating layer 316 may have a thickness of about 25 nm to about 2500 nm. The thickness of metallic coating layer 316 may vary over the surface of particle core 314, but will preferably have a substantially uniform thickness over the surface of particle core 314. Metallic coating layer 316 may include a single layer, as illustrated in
Metallic coating layer 316 and coating material 320 have a melting temperature (TC). As used herein, TC includes the lowest temperature at which incipient melting or liquation or other forms of partial melting occur within coating material 320, regardless of whether coating material 320 comprises a pure metal, an alloy with multiple phases each having different melting temperatures or a composite, including a composite comprising a plurality of coating material layers having different melting temperatures.
Metallic coating material 320 may include any suitable metallic coating material 320 that provides a sinterable outer surface 321 that is configured to be sintered to an adjacent powder particle 312 that also has a metallic coating layer 316 and sinterable outer surface 321. In powders 310 that also include second or additional (coated or uncoated) particles, as described herein, the sinterable outer surface 321 of metallic coating layer 316 is also configured to be sintered to a sinterable outer surface 321 of second particles. In an exemplary embodiment, the powder particles 312 are sinterable at a predetermined sintering temperature (TS) that is a function of the core material 318 and coating material 320, such that sintering of powder compact 400 is accomplished entirely in the solid state and where TS is less than TP and TC. Sintering in the solid state limits particle core 314/metallic coating layer 316 interactions to solid state diffusion processes and metallurgical transport phenomena and limits growth of and provides control over the resultant interface between them. In contrast, for example, the introduction of liquid phase sintering would provide for rapid interdiffusion of the particle core 314/metallic coating layer 316 materials and make it difficult to limit the growth of and provide control over the resultant interface between them, and thus interfere with the formation of the desirable microstructure of particle compact 400 as described herein.
In an exemplary embodiment, core material 318 will be selected to provide a core chemical composition and the coating material 320 will be selected to provide a coating chemical composition and these chemical compositions will also be selected to differ from one another. In another exemplary embodiment, the core material 318 will be selected to provide a core chemical composition and the coating material 320 will be selected to provide a coating chemical composition and these chemical compositions will also be selected to differ from one another at their interface. Differences in the chemical compositions of coating material 320 and core material 318 may be selected to provide different dissolution rates and selectable and controllable dissolution of powder compacts 400 that incorporate them making them selectably and controllably dissolvable. This includes dissolution rates that differ in response to a changed condition in the borehole, including an indirect or direct change in a borehole fluid. In an exemplary embodiment, a powder compact 400 formed from powder 310 having chemical compositions of core material 318 and coating material 320 that make compact 400 is selectably dissolvable in a borehole fluid in response to a changed borehole condition that includes a change in temperature, change in pressure, change in flow rate, change in pH or change in chemical composition of the borehole fluid, or a combination thereof. The selectable dissolution response to the changed condition may result from actual chemical reactions or processes that promote different rates of dissolution, but also encompass changes in the dissolution response that are associated with physical reactions or processes, such as changes in borehole fluid pressure or flow rate.
As illustrated in
As used herein, the use of the term substantially-continuous cellular nanomatrix 416 does not connote the major constituent of the powder compact, but rather refers to the minority constituent or constituents, whether by weight or by volume. This is distinguished from most matrix composite materials where the matrix comprises the majority constituent by weight or volume. The use of the term substantially-continuous, cellular nanomatrix is intended to describe the extensive, regular, continuous and interconnected nature of the distribution of nanomatrix material 420 within powder compact 400. As used herein, “substantially-continuous” describes the extension of the nanomatrix material throughout powder compact 400 such that it extends between and envelopes substantially all of the dispersed particles 414. Substantially-continuous is used to indicate that complete continuity and regular order of the nanomatrix around each dispersed particle 414 is not required. For example, defects in the coating layer 316 over particle core 314 on some powder particles 312 may cause bridging of the particle cores 214 during sintering of the powder compact 400, thereby causing localized discontinuities to result within the cellular nanomatrix 416, even though in the other portions of the powder compact the nanomatrix is substantially continuous and exhibits the structure described herein. As used herein, “cellular” is used to indicate that the nanomatrix defines a network of generally repeating, interconnected, compartments or cells of nanomatrix material 420 that encompass and also interconnect the dispersed particles 414. As used herein, “nanomatrix” is used to describe the size or scale of the matrix, particularly the thickness of the matrix between adjacent dispersed particles 414. The metallic coating layers that are sintered together to form the nanomatrix are themselves nanoscale thickness coating layers. Since the nanomatrix at most locations, other than the intersection of more than two dispersed particles 414, generally comprises the interdiffusion and bonding of two coating layers 316 from adjacent powder particles 312 having nanoscale thicknesses, the matrix formed also has a nanoscale thickness (e.g., approximately two times the coating layer thickness as described herein) and is thus described as a nanomatrix. Further, the use of the term dispersed particles 414 does not connote the minor constituent of powder compact 400, but rather refers to the majority constituent or constituents, whether by weight or by volume. The use of the term dispersed particle is intended to convey the discontinuous and discrete distribution of particle core material 418 within powder compact 400.
Powder compact 400 may have any desired shape or size, including that of a cylindrical billet or bar that may be machined or otherwise used to form useful articles of manufacture, including the dissolvable inserts 252. The pressing used to form precursor powder compact and sintering and pressing processes used to form powder compact 400 and deform the powder particles 312, including particle cores 314 and coating layers 316, to provide the full density and desired macroscopic shape and size of powder compact 400 as well as its microstructure. The microstructure of powder compact 400 includes an equiaxed configuration of dispersed particles 414 that are dispersed throughout and embedded within the substantially-continuous, cellular nanomatrix 416 of sintered coating layers. This microstructure is somewhat analogous to an equiaxed grain microstructure with a continuous grain boundary phase, except that it does not require the use of alloy constituents having thermodynamic phase equilibria properties that are capable of producing such a structure. Rather, this equiaxed dispersed particle structure and cellular nanomatrix 416 of sintered metallic coating layers 316 may be produced using constituents where thermodynamic phase equilibrium conditions would not produce an equiaxed structure. The equiaxed morphology of the dispersed particles 414 and cellular network 416 of particle layers results from sintering and deformation of the powder particles 312 as they are compacted and interdiffuse and deform to fill the interparticle spaces 315 (
In an exemplary embodiment as illustrated in
As nanomatrix 416 is formed, including bond 417 and bond layer 419, the chemical composition or phase distribution, or both, of metallic coating layers 316 may change. Nanomatrix 416 also has a melting temperature (TM). As used herein, TM includes the lowest temperature at which incipient melting or liquation or other forms of partial melting will occur within nanomatrix 416, regardless of whether nanomatrix material 420 comprises a pure metal, an alloy with multiple phases each having different melting temperatures or a composite, including a composite comprising a plurality of layers of various coating materials having different melting temperatures, or a combination thereof, or otherwise. As dispersed particles 414 and particle core materials 418 are formed in conjunction with nanomatrix 416, diffusion of constituents of metallic coating layers 316 into the particle cores 314 is also possible, which may result in changes in the chemical composition or phase distribution, or both, of particle cores 314. As a result, dispersed particles 414 and particle core materials 418 may have a melting temperature (TDP) that is different than TP. As used herein, TDP includes the lowest temperature at which incipient melting or liquation or other forms of partial melting will occur within dispersed particles 414, regardless of whether particle core material 418 comprise a pure metal, an alloy with multiple phases each having different melting temperatures or a composite, or otherwise. Powder compact 400 is formed at a sintering temperature (TS), where TS is less than TC, TP, TM and TDP.
Dispersed particles 414 may comprise any of the materials described herein for particle cores 314, even though the chemical composition of dispersed particles 414 may be different due to diffusion effects as described herein. In an exemplary embodiment, dispersed particles 414 are formed from particle cores 314 comprising materials having a standard oxidation potential greater than or equal to Zn, including Mg, Al, Zn or Mn, or a combination thereof, may include various binary, tertiary and quaternary alloys or other combinations of these constituents as disclosed herein in conjunction with particle cores 314. Of these materials, those having dispersed particles 414 comprising Mg and the nanomatrix 416 formed from the metallic coating materials 316 described herein are particularly useful. Dispersed particles 414 and particle core material 418 of Mg, Al, Zn or Mn, or a combination thereof, may also include a rare earth element, or a combination of rare earth elements as disclosed herein in conjunction with particle cores 314.
In another exemplary embodiment, dispersed particles 414 are formed from particle cores 314 comprising metals that are less electrochemically active than Zn or non-metallic materials. Suitable non-metallic materials include ceramics, glasses (e.g., hollow glass microspheres) or carbon, or a combination thereof, as described herein.
Dispersed particles 414 of powder compact 400 may have any suitable particle size, including the average particle sizes described herein for particle cores 414.
Dispersed particles 314 may have any suitable shape depending on the shape selected for particle cores 314 and powder particles 312, as well as the method used to sinter and compact powder 310. In an exemplary embodiment, powder particles 312 may be spheroidal or substantially spheroidal and dispersed particles 414 may include an equiaxed particle configuration as described herein.
The nature of the dispersion of dispersed particles 414 may be affected by the selection of the powder 310 or powders 310 used to make particle compact 400. In one exemplary embodiment, a powder 310 having a unimodal distribution of powder particle 312 sizes may be selected to form powder compact 400 and will produce a substantially homogeneous unimodal dispersion of particle sizes of dispersed particles 414 within cellular nanomatrix 416, as illustrated generally in
Nanomatrix 416 is a substantially-continuous, cellular network of metallic coating layers 316 that are sintered to one another. The thickness of nanomatrix 416 will depend on the nature of the powder 310 or powders 310 used to form powder compact 400, as well as the incorporation of any second powder, particularly the thicknesses of the coating layers associated with these particles. In an exemplary embodiment, the thickness of nanomatrix 416 is substantially uniform throughout the microstructure of powder compact 400 and comprises about two times the thickness of the coating layers 316 of powder particles 312. In another exemplary embodiment, the cellular network 416 has a substantially uniform average thickness between dispersed particles 414 of about 50 nm to about 5000 nm.
Nanomatrix 416 is formed by sintering metallic coating layers 316 of adjacent particles to one another by interdiffusion and creation of bond layer 419 as described herein. Metallic coating layers 316 may be single layer or multilayer structures, and they may be selected to promote or inhibit diffusion, or both, within the layer or between the layers of metallic coating layer 316, or between the metallic coating layer 316 and particle core 314, or between the metallic coating layer 316 and the metallic coating layer 316 of an adjacent powder particle, the extent of interdiffusion of metallic coating layers 316 during sintering may be limited or extensive depending on the coating thicknesses, coating material or materials selected, the sintering conditions and other factors. Given the potential complexity of the interdiffusion and interaction of the constituents, description of the resulting chemical composition of nanomatrix 416 and nanomatrix material 420 may be simply understood to be a combination of the constituents of coating layers 316 that may also include one or more constituents of dispersed particles 414, depending on the extent of interdiffusion, if any, that occurs between the dispersed particles 414 and the nanomatrix 416. Similarly, the chemical composition of dispersed particles 414 and particle core material 418 may be simply understood to be a combination of the constituents of particle core 314 that may also include one or more constituents of nanomatrix 416 and nanomatrix material 420, depending on the extent of interdiffusion, if any, that occurs between the dispersed particles 414 and the nanomatrix 416.
In an exemplary embodiment, the nanomatrix material 420 has a chemical composition and the particle core material 418 has a chemical composition that is different from that of nanomatrix material 420, and the differences in the chemical compositions may be configured to provide a selectable and controllable dissolution rate, including a selectable transition from a very low dissolution rate to a very rapid dissolution rate, in response to a controlled change in a property or condition of the borehole proximate the compact 400, including a property change in a borehole fluid that is in contact with the powder compact 400, as described herein. Nanomatrix 416 may be formed from powder particles 312 having single layer and multilayer coating layers 316. This design flexibility provides a large number of material combinations, particularly in the case of multilayer coating layers 316, that can be utilized to tailor the cellular nanomatrix 416 and composition of nanomatrix material 420 by controlling the interaction of the coating layer constituents, both within a given layer, as well as between a coating layer 316 and the particle core 314 with which it is associated or a coating layer 316 of an adjacent powder particle 312. Several exemplary embodiments that demonstrate this flexibility are provided below.
As illustrated in
In another exemplary embodiment, powder compact 400 is formed from powder particles 312 where the coating layer 316 comprises a multilayer coating layer 316 having a plurality of coating layers, and the resulting nanomatrix 416 between adjacent ones of the plurality of dispersed particles 414 comprises the plurality of layers (t) comprising the coating layer 316 of one particle 312, a bond layer 419, and the plurality of layers comprising the coating layer 316 of another one of powder particles 312. In
Sintered and forged powder compacts 400 that include dispersed particles 414 comprising Mg and nanomatrix 416 comprising various nanomatrix materials as described herein have demonstrated an excellent combination of mechanical strength and low density that exemplify the lightweight, high-strength materials disclosed herein. Examples of powder compacts 400 that have pure Mg dispersed particles 414 and various nanomatrices 416 formed from powders 310 having pure Mg particle cores 314 and various single and multilayer metallic coating layers 316 that include Al, Ni, W or Al2O3, or a combination thereof. These powders compacts 400 have been subjected to various mechanical and other testing, including density testing, and their dissolution and mechanical property degradation behavior has also been characterized as disclosed herein. The results indicate that these materials may be configured to provide a wide range of selectable and controllable corrosion or dissolution behavior from very low corrosion rates to extremely high corrosion rates, particularly corrosion rates that are both lower and higher than those of powder compacts that do not incorporate the cellular nanomatrix, such as a compact formed from pure Mg powder through the same compaction and sintering processes in comparison to those that include pure Mg dispersed particles in the various cellular nanomatrices described herein. These powder compacts 400 may also be configured to provide substantially enhanced properties as compared to powder compacts formed from pure Mg particles that do not include the nanoscale coatings described herein. Powder compacts 400 that include dispersed particles 414 comprising Mg and nanomatrix 416 comprising various nanomatrix materials 420 described herein have demonstrated room temperature compressive strengths of at least about 37 ksi, and have further demonstrated room temperature compressive strengths in excess of about 50 ksi, both dry and immersed in a solution of 3% KCl at 200° F. In contrast, powder compacts formed from pure Mg powders have a compressive strength of about 20 ksi or less. Strength of the nanomatrix powder metal compact 400 can be further improved by optimizing powder 310, particularly the weight percentage of the nanoscale metallic coating layers 316 that are used to form cellular nanomatrix 416. Strength of the nanomatrix powder metal compact 400 can be further improved by optimizing powder 310, particularly the weight percentage of the nanoscale metallic coating layers 316 that are used to form cellular nanomatrix 416. For example, varying the weight percentage (wt. %), i.e., thickness, of an alumina coating within a cellular nanomatrix 416 formed from coated powder particles 312 that include a multilayer (Al/Al2O3/Al) metallic coating layer 316 on pure Mg particle cores 314 provides an increase of 21% as compared to that of 0 wt % alumina.
Powder compacts 400 comprising dispersed particles 414 that include Mg and nanomatrix 416 that includes various nanomatrix materials as described herein have also demonstrated a room temperature sheer strength of at least about 20 ksi. This is in contrast with powder compacts formed from pure Mg powders, which have room temperature sheer strengths of about 8 ksi.
Powder compacts 400 of the types disclosed herein are able to achieve an actual density that is substantially equal to the predetermined theoretical density of a compact material based on the composition of powder 310, including relative amounts of constituents of particle cores 314 and metallic coating layer 316, and are also described herein as being fully-dense powder compacts. Powder compacts 400 comprising dispersed particles that include Mg and nanomatrix 416 that includes various nanomatrix materials as described herein have demonstrated actual densities of about 1.738 g/cm3 to about 2.50 g/cm3, which are substantially equal to the predetermined theoretical densities, differing by at most 4% from the predetermined theoretical densities.
Powder compacts 400 as disclosed herein may be configured to be selectively and controllably dissolvable in a borehole fluid in response to a changed condition in a borehole. Examples of the changed condition that may be exploited to provide selectable and controllable dissolvability include a change in temperature, change in pressure, change in flow rate, change in pH or change in chemical composition of the borehole fluid, or a combination thereof. An example of a changed condition comprising a change in temperature includes a change in borehole fluid temperature. For example, powder compacts 400 comprising dispersed particles 414 that include Mg and cellular nanomatrix 416 that includes various nanomatrix materials as described herein have relatively low rates of corrosion in a 3% KCl solution at room temperature that range from about 0 to about 11 mg/cm2/hr as compared to relatively high rates of corrosion at 200° F. that range from about 1 to about 246 mg/cm2/hr depending on different nanoscale coating layers 216. An example of a changed condition comprising a change in chemical composition includes a change in a chloride ion concentration or pH value, or both, of the borehole fluid. For example, powder compacts 400 comprising dispersed particles 414 that include Mg and nanomatrix 416 that includes various nanoscale coatings described herein demonstrate corrosion rates in 15% HCl that range from about 4750 mg/cm2/hr to about 7432 mg/cm2/hr. Thus, selectable and controllable dissolvability in response to a changed condition in the borehole, namely the change in the borehole fluid chemical composition from KCl to HCl, may be used to achieve a characteristic response as illustrated graphically in
Without being limited by theory, powder compacts 400 are formed from coated powder particles 312 that include a particle core 314 and associated core material 318 as well as a metallic coating layer 316 and an associated metallic coating material 320 to form a substantially-continuous, three-dimensional, cellular nanomatrix 416 that includes a nanomatrix material 420 formed by sintering and the associated diffusion bonding of the respective coating layers 316 that includes a plurality of dispersed particles 414 of the particle core materials 418. This unique structure may include metastable combinations of materials that would be very difficult or impossible to form by solidification from a melt having the same relative amounts of the constituent materials. The coating layers and associated coating materials may be selected to provide selectable and controllable dissolution in a predetermined fluid environment, such as a borehole environment, where the predetermined fluid may be a commonly used borehole fluid that is either injected into the borehole or extracted from the borehole. As will be further understood from the description herein, controlled dissolution of the nanomatrix exposes the dispersed particles of the core materials. The particle core materials may also be selected to also provide selectable and controllable dissolution in the borehole fluid. Alternately, they may also be selected to provide a particular mechanical property, such as compressive strength or sheer strength, to the powder compact 400, without necessarily providing selectable and controlled dissolution of the core materials themselves, since selectable and controlled dissolution of the nanomatrix material surrounding these particles will necessarily release them so that they are carried away by the borehole fluid. The microstructural morphology of the substantially-continuous, cellular nanomatrix 416, which may be selected to provide a strengthening phase material, with dispersed particles 414, which may be selected to provide equiaxed dispersed particles 414, provides these powder compacts with enhanced mechanical properties, including compressive strength and sheer strength, since the resulting morphology of the nanomatrix/dispersed particles can be manipulated to provide strengthening through the processes that are akin to traditional strengthening mechanisms, such as grain size reduction, solution hardening through the use of impurity atoms, precipitation or age hardening and strength/work hardening mechanisms. The nanomatrix/dispersed particle structure tends to limit dislocation movement by virtue of the numerous particle nanomatrix interfaces, as well as interfaces between discrete layers within the nanomatrix material as described herein. This is exemplified in the fracture behavior of these materials. A powder compact 400 made using uncoated pure Mg powder and subjected to a shear stress sufficient to induce failure demonstrated intergranular fracture. In contrast, a powder compact 400 made using powder particles 312 having pure Mg powder particle cores 314 to form dispersed particles 414 and metallic coating layers 316 that includes Al to form nanomatrix 416 and subjected to a shear stress sufficient to induce failure demonstrated transgranular fracture and a substantially higher fracture stress as described herein. Because these materials have high-strength characteristics, the core material and coating material may be selected to utilize low density materials or other low density materials, such as low-density metals, ceramics, glasses or carbon, that otherwise would not provide the necessary strength characteristics for use in the desired applications, including borehole tools and components.
With respect to
As shown in
While two additional fracture order of operations have been described, it should be understood that the selective hydraulic fracturing tool may be utilized to fracture zones of the borehole in any order deemed appropriate by the operator or borehole conditions.
While the invention has been described with reference to an exemplary embodiment or embodiments, it will be understood by those skilled in the art that various changes may be made and equivalents may be substituted for elements thereof without departing from the scope of the invention. In addition, many modifications may be made to adapt a particular situation or material to the teachings of the invention without departing from the essential scope thereof. Therefore, it is intended that the invention not be limited to the particular embodiment disclosed as the best mode contemplated for carrying out this invention, but that the invention will include all embodiments falling within the scope of the claims. Also, in the drawings and the description, there have been disclosed exemplary embodiments of the invention and, although specific terms may have been employed, they are unless otherwise stated used in a generic and descriptive sense only and not for purposes of limitation, the scope of the invention therefore not being so limited. Moreover, the use of the terms first, second, etc. do not denote any order or importance, but rather the terms first, second, etc. are used to distinguish one element from another. Furthermore, the use of the terms a, an, etc. do not denote a limitation of quantity, but rather denote the presence of at least one of the referenced item.
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