The disclosure relates generally to cutting elements for earth-boring tools. More specifically, the disclosed embodiments relate to cutting elements that may be self-sharpening, earth-boring tools including such self-sharpening cutting elements, and methods of forming self-sharpening cutting elements.
Earth-boring tools for forming wellbores in subterranean earth formations may include a plurality of cutting elements secured to a body. For example, fixed-cutter earth-boring rotary drill bits (also referred to as “drag bits”) include a plurality of cutting elements that are fixedly attached to a bit body of the drill bit. Similarly, roller cone earth-boring rotary drill bits may include cones that are mounted on bearing pins extending from legs of a bit body such that each cone is capable of rotating about the bearing pin on which it is mounted. A plurality of cutting elements may be mounted to each cone of the drill bit.
The cutting elements used in such earth-boring tools often include polycrystalline diamond cutters (often referred to as “PDCs”), which are cutting elements that include a polycrystalline diamond (PCD) material. Such polycrystalline diamond cutting elements are formed by sintering and bonding together relatively small diamond grains or crystals under conditions of high temperature and high pressure in the presence of a catalyst (such as, for example, cobalt, iron, nickel, or alloys and mixtures thereof) to form a layer of polycrystalline diamond material on a cutting element substrate. These processes are often referred to as high temperature/high pressure (or “HTHP”) processes. The cutting element substrate may comprise a cermet material (i.e., a ceramic-metal composite material) such as cobalt-cemented tungsten carbide. In such instances, the cobalt (or other catalyst material) in the cutting element substrate may be drawn into the diamond grains or crystals during sintering and serve as a catalyst material for forming a diamond table from the diamond grains or crystals. In other methods, powdered catalyst material may be mixed with the diamond grains or crystals prior to sintering the grains or crystals together in an HTHP process.
PDC cutting elements commonly have a planar, disc-shaped diamond table on an end surface of a cylindrical cemented carbide substrate. Such a PDC cutting element may be mounted to an earth-boring rotary drag bit or other tool using fixed PDC cutting elements in a position and orientation that causes a peripheral edge of the diamond table to scrape against and shear away the surface of the formation being cut as the drill bit is rotated within a wellbore. As the PDC cutting element wears, a so-called “wear scar” or “wear flat” develops that comprises a generally flat surface of the cutting element that ultimately may extend from the front, exposed major surface of the diamond table to the cylindrical lateral side surface of the cemented carbide substrate.
Early PDC cutting elements had relatively thinner diamond tables having an average thickness of about one (1) millimeter or less. As such cutting elements were used to cut formation material, the wear scar that developed often included an uneven profile wherein the surface of the diamond table that was rubbing against the formation projected outward from the cutting element beyond the adjacent surface of the cemented carbide substrate that was rubbing against the formation. It was believed that this phenomenon was due to the fact that the rubbing surface of the cemented carbide substrate was wearing at a faster rate than was the rubbing surface of the diamond table. The portion of the diamond table at the wear scar projecting outward beyond the adjacent rubbing surface of the cemented carbide substrate has been referred to as a “shear lip.” The formation of such a shear lip may beneficially result in an increased rate of penetration (ROP).
In some embodiments, cutting elements for earth-boring tools comprise a substrate comprising at least one material selected from the group consisting of CoCr, CoCrMo, CoCrW, and Ti. A polycrystalline superabrasive material may be attached to the substrate.
In other embodiments, earth-boring tools comprise a body. At least one cutting element is attached to the body. The cutting element comprises or the cutting elements comprise a substrate comprising at least one material selected from the group consisting of CoCr, CoCrMo, CoCrW, and Ti. A polycrystalline superabrasive material may be attached to the substrate.
In still other embodiments, methods of foci ling cutting elements for earth-boring tools comprise disposing a substrate comprising at least one material selected from the group consisting of CoCr, CoCrMo, CoCrW, and Ti in a container. Particles of superabrasive material may be disposed in the container. The particles of superabrasive material may be sintered with the substrate in the container to form a polycrystalline superabrasive material attached to the substrate.
While the specification concludes with claims particularly pointing out and distinctly claiming what are regarded as embodiments of the invention, various features and advantages of disclosed embodiments may be more readily ascertained from the following description when read in conjunction with the accompanying drawings, in which:
The illustrations presented herein are not meant to be actual views of any particular cutting element, container, earth-boring tool, or component thereof, but are merely idealized representations employed to describe illustrative embodiments. Thus, the drawings are not necessarily to scale. Additionally, elements common between figures may retain the same or similar numerical designation.
Disclosed embodiments relate generally to cutting elements that may be self-sharpening. More specifically, disclosed are cutting element substrates that may comprise, for example, at least one of CoCr, CoCrMo, CoCrW, and elemental Ti, which may enable the cutting elements including such substrates to be self-sharpening.
As used herein, the term “superabrasive material” means and includes any material having a Knoop hardness value of about 3,000 Kgf/mm2 (29,420 MPa) or more. Superabrasive materials include, for example, diamond and cubic boron nitride. Superabrasive materials may also be characterized as “superhard” materials.
As used herein, the term “polycrystalline material” means and includes any material comprising a plurality of grains (i.e., crystals) of material that are bonded directly together by inter-granular bonds. The crystal structures of the individual grains of the material may be randomly oriented in space within the polycrystalline material.
As used herein, the terms “inter-granular bond” and “interbonded” mean and include any direct atomic bond (e.g., covalent, ionic, etc.) between atoms in adjacent grains of superabrasive material.
The term “sintering,” as used herein, means temperature driven mass transport resulting in densification of a particulate component, and typically involves removal of at least a portion of the pores between the starting particles (accompanied by shrinkage) combined with coalescence and bonding among adjacent particles.
As used herein, the term “material composition” means the chemical composition and microstructure of a material. In other words, materials having the same chemical composition but a different microstructure have different material compositions.
Referring to
A material 24 of the cutting table 12 may comprise a polycrystalline superabrasive material. For example, the material 24 of the cutting table 12 may comprise polycrystalline diamond (e.g., synthetic diamond, natural diamond, or synthetic and natural diamond), cubic boron nitride, carbon nitrides, boron carbon nitride, and other polycrystalline superabrasive materials known in the art.
A material 26 of the substrate 14 may wear at a faster rate than cobalt-cemented tungsten carbide. For example, the material 26 of the substrate 14 may comprise a metal, a metal alloy, or a particle matrix composite. More specifically, the substrate 14 may comprise, for example, at least one material 26 selected from the group consisting of CoCr, CoCrMo, CoCrW, and Ti. A substrate 14 comprising CoCr may comprise, for example, ASTM F-799, ASTM F-90, ASTM F-75, or ASTM F-562. A substrate 14 comprising Ti may comprise, for example, commercially pure Ti, Ti6A14V, ASTM F-1313, ASTM F-620, ASTM F-1580, TiMbHf, or Nitinol. The substrate 14 may enable the cutting element 10 to be self-sharpening due, at least in part, to the relatively high wear rate of the substrate 14 during cutting action, as discussed below with reference to
In previously known cutting elements comprising cobalt-cemented tungsten carbide substrates, the relatively high wear resistance of the cobalt-cemented tungsten carbide may cause the cutting element to present a dull cutting edge upon wear of the cutting element to a degree, and/or after chipping or spalling of the cutting table has occurred. As a result, the weight-on-bit required to maintain a given depth-of-cut may increase, and/or a torque required to continue rotating an earth-boring tool to which the cutting element is attached may increase, even to the point where the earth-boring tool may become stuck or jammed in the wellbore and require expensive and time-consuming removal techniques.
Referring again to
In some embodiments, the substrate 14 may be at least substantially free of particle-matrix composite material. When it is said that the substrate 14 may be at least substantially free of particle-matrix composite material, it is meant that the material 26 of the substrate 14 may be free of particle-matrix composite material other than particle-matrix composite materials that may be inherently formed by the material 24 of the cutting table 12 and the material 26 of the substrate 14 during formation of the cutting element 10by, for example, migration of particles from the material 24 of the cutting table 12 into the material 26 of the substrate 14 proximate the interface 18. For example, the substrate 14 may comprise a metal or a metal alloy. More specifically, the substrate 14 may comprise, for example, a material 26 comprising at least one metal or metal alloy selected from the group consisting of CoCr, CoCrMo, CoCrW, Ti, and alloys thereof.
In some embodiments, the substrate 14 may comprise a particle-matrix composite material. In such embodiments, the matrix of the particle-matrix composite material may comprise, for example, a material selected from the group consisting of CoCr, CoCrMo, CoCrW, and Ti, such as, for example, any of the alloys discussed previously herein. The particles dispersed among the matrix of the particle-matrix composite material may comprise hard ceramics, such as, for example, carbides and borides made from elements such as W, Ti, Mo, Nb, V, Hf, Ta, Cr, Zr, Al, and Si.
Referring to
An interface 18′ between the cutting table 12 and the substrate 14 may be non-planar in some embodiments, which may increase a strength of the attachment of the cutting table 12 to the substrate 14. For example, the substrate 14 may include at least one protrusion 28 and the cutting table 12 may include at least one recess 30 into which the protrusion may be at least partially inserted. As a specific, non-limiting example, the protrusion 28 may be dome-shaped and may extend from the end 16 of the substrate 14, and the recess 30 may be correspondingly dome-shaped and conform to the contour of the protrusion 28. As other examples, the substrate 14 may include at least one recess and the cutting table 12 may include at least one protrusion at least partially inserted therein or the substrate 14 may include at least one recess and at least one protrusion and the cutting table 12 may include at least one corresponding protrusion and at least one corresponding recess, respectively. Such non-planar interface features may be in any configuration known in the art. Features of the interface 18′ may be configured to increase the degree self-sharpening of the cutting element 10′ as the cutting edge 19 (see
Referring to
Referring to
Particles of superabrasive material 38 may be disposed in the container 34. The particles of superabrasive material 38 may comprise, for example, diamond grains, particles of cubic boron nitride, or particles of other superabrasive materials known in the art. The particles of superabrasive material 38 may exhibit a monomodal or a multimodal (e.g., bimodal, trimodal, etc.) particle size distribution, may be distributed such that different regions of the particles of superabrasive material 38 within the container 34 comprise different average particle sizes, and may exhibit a gradient in average particle size passing through different regions of the particles of superabrasive material 38 within the container 34. In some embodiments, a catalyst material 40, which may catalyze formation of particle-to-particle bonds among the particles of superabrasive material 38, may be dispersed among the particles of superabrasive material 38 in the container. For example, powdered catalyst material 40 may be admixed with the particles of superabrasive material 38 and the resulting mixture of particles may be disposed in the container 34. The catalyst material 40 may comprise, for example, Co, Fe, Ni, alloys and mixtures thereof, or other catalyst materials 40 known in the art. In other embodiments, catalyst material may be swept from the substrate 14 among the particles of superabrasive material 38 to catalyze formation of particle-to-particle bonds among the particles of superabrasive material 38. For example, where the material 26 of the substrate 14 comprises CoCr, CoCrMo, or CoCrW, the material 26 of the substrate 14 (e.g., the Co constituent of the material 26) may catalyze formation of particle-to-particle bonds among the particles of superabrasive material 38.
In some embodiments, an intermediate material 32 may be disposed in the container 34 between the substrate 14 and the particles of superabrasive material 38. For example, a layer 42 (e.g., a foil) of the intermediate material 32 may be located between the substrate 14 and the particles of superabrasive material 38 in the container 34. In other embodiments, the substrate 14 may abut the particles of superabrasive material 38 directly, there being no intermediate material 32 interposed therebetween.
The particles of superabrasive material 38 may be sintered with the substrate 14 in the container 34 to form a polycrystalline superabrasive material 24 (see
For example, the substrate 14 may plasticize, catalyst material from the material 26 of the substrate 14 may be swept among the particles of superabrasive material 38, direct particle-to-particle bonds may form among the particles of superabrasive material 38 to form a polycrystalline superabrasive material 24 (see
In some embodiments, at least some material located in interstitial spaces among interbonded particles 38 of the polycrystalline superabrasive material 24 may be removed. For example, material 26 of the substrate 14 that has swept into the interstitial spaces, intermediate material 32 that has swept into the interstitial spaces, or catalyst material 40 located in the interstitial spaces may be removed from all or a portion of the polycrystalline superabrasive material 24. For example, leaching processes known in the art may be used to remove material located in the interstitial spaces from regions of the polycrystalline superabrasive material 24 at and near the cutting face 22 (see
Referring to
While certain illustrative embodiments have been described in connection with the figures, those of ordinary skill in the art will recognize and appreciate that embodiments of the invention are not limited to those embodiments explicitly shown and described herein. Rather, many additions, deletions, and modifications to the embodiments described herein may be made without departing from the scope of embodiments of the invention as hereinafter claimed, including legal equivalents. In addition, features from one disclosed embodiment may be combined with features of another disclosed embodiment while still being encompassed within the scope of embodiments of the invention as contemplated by the inventor.
This application claims the benefit of U.S. Provisional patent application Ser. No. 61/613,846, filed Mar. 21, 2012, and of U.S. Provisional patent application Ser. No. 61/619,121, filed Apr. 2, 2012, the disclosure of each of which is incorporated herein in its entirety by this reference.
Number | Date | Country | |
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61613846 | Mar 2012 | US | |
61619121 | Apr 2012 | US |