The present disclosure relates generally to cutting elements and other downhole drilling components that include thermally stable polycrystalline materials usable in connection with wellbore drilling and systems and methods of manufacture using anodic bonding.
Rotary drill bits are frequently used to drill oil and gas wells, geothermal wells, and water wells. Fixed cutter drill bits or drag bits are often formed with a bit body having cutting elements or inserts disposed at select locations of exterior portions of the bit body. Drill bits and other downhole equipment may also have a variety of other abrasive and/or wear-resistant, hardfacing elements. Cutting elements and hardfacing elements can be made from polycrystalline materials.
For example, cutting elements having a polycrystalline cutting layer (or table) have been used in industrial applications including wellbore drilling and metal machining for many years. One such material is a polycrystalline diamond (PCD), which is a polycrystalline mass of diamonds (typically synthetic) that is bonded together to form an integral, tough, high-strength mass. To form a cutting element, a cutting layer is bonded to a substrate material, which is typically a sintered metal-carbide. When bonded to a substrate, a PCD is referred to as a polycrystalline diamond compact (PDC). Polycrystalline materials for use in cutting elements or hardfacing structural elements can also be made from other polycrystallline materials such as polycrystalline cubic boron nitride (PCBN).
Methods for securing thermally stable polycrystalline material to a substrate for use in drill bit cutting element, or other abrasive and/or wear-resistant, hardfacing structural element that are part of a drill bit body or other downhole equipment have been actively investigated. High temperature high pressure (HTHP) processing is a common method of attachment. However, this method typically uses another catalyst, such as cobalt, and results in reduced thermal stability of the polycrystalline material.
Certain embodiments and features of the present disclosure relate to cutting elements and hardfacing components of drill bits and other downhole equipment that include thermally stable polycrystalline material and can be used in connection with wellbore drilling and systems, as well as methods of manufacturing such elements using anodic bonding. In some examples, a cutting element having a thermally stable polycrystalline material cutting layer can be attached to a drill bit head or other downhole equipment, such as a reamer or a hole opener, that can be used to break apart, cut, or crush rock and earth formations when drilling a wellbore, such as those drilled to extract water, gas, or oil. In another example, a hardfacing component having a thermally stable polycrystalline material outer-facing layer can be attached to a drill bit or other downhole equipment. Such hardfacing components may be wear-resistant, reducing susceptibility of the drill bit or downhole equipment to damage due to frictional heat and may facilitate movement of the equipment downhole during use. Examples of hardfacing components include drill bit heads, gage protectors, and impact arrestors. An electrical field can be used to covalently bond the thermally stable polycrystalline material to a substrate to form the cutting element or hardfacing component. In some examples, anodic bonding of the thermally stable polycrystalline material to the substrate or hardfacing component maximizes the thermal stability of the cutting element or hardfacing component. As a result, the cutting element or hardfacing component can have improved thermo-mechanical integrity and abrasion resistance, and has reduced leaching exposure compared to those made using conventional methods of attaching a cutting layer to a substrate.
A PCD includes individual diamond “crystals” that are interconnected in a lattice structure. A metal catalyst (in particular, Group VIII metal catalysts), such as cobalt, has been used to promote recrystallization of the diamond particles and formation of the lattice structure (for example, in a sintering process). However, Group VIII metal catalysts have significantly different coefficient of thermal expansion (CTE) as compared to diamond and, upon heating a PCD, the metal catalyst and the diamond lattice will expand at different rates, causing cracks to form in the lattice structure and resulting in deterioration of the cutting layer (during downhole use). Also, at elevated temperatures (>800° C.) and in the absence of elevated pressure, the metal catalyst will also revert the diamond to graphite. In order to obviate this problem, strong acids may be used to “leach” the cobalt from the diamond lattice structure, generating a thermally stable polycrystalline diamond material. Similar issues occur and must be addressed for other polycrystalline materials. Cutting elements with a cutting layer of thermally stable polycrystalline material have relatively low wear rates, even as cutter temperatures reach 1200° C.
In some cases, the polycrystalline material is made of diamond or other superhard particles bound together with a binder (for example, silicon) in a matrix composite. Hardfacing components may include this type of polycrystalline material as an abrasive and/or wear-resistant feature.
For simplicity, features of a drill bit cutting element that includes a thermally stable polycrystalline material cutting layer made from a polycrystalline diamond (PCD), along with systems and methods for making and using this component, are described in detail. However, such features similarly relate to abrasive or wear-bearing hardfacing components of a drill bit or other downhole equipment, along with systems and methods for making and using such components. Such features also similarly relate to components containing other polycrystalline materials, along with systems and methods for making and using such components.
In one example, a cutting element that includes a cutting layer made of thermally stable polycrystalline material anodically bonded to a substrate is attached to a drill bit for earth formation drilling. A fixed cutter drill bit 10 having such cutting elements is shown in
In another example, a cutting element 20 that includes a thermally stable polycrystalline material anodically bonded to a substrate is shown in
For example, the cutting layer 24 can include a thermally stable polycrystalline material. The thermally stable polycrystalline material may include polycrystalline diamond, polycrystalline cubic boron nitride, or another super abrasive material. The substrate 22 may be a carbide or a metal. For example, the carbide may include cemented tungsten carbide (WC), silicon carbide (SiC), or another super hard material. Where the substrate 22 is a metal, the metal may include steel, a nickel/iron alloy, Invar, or titanium. Examples of substrates include metals (for example, steel, invar, titanium, etc.), silicon-coated metals, silicon-coated and cemented tungsten carbide, and silicon carbide. Either or both of the cutting layer 24 and the substrate 22 can be plated, layered, or coated with metal or silicon to facilitate the anodic bonding process. In some examples, the substrate 22 may be a carbide or a metal that includes, or is covalently coated with, silicon.
The cutting layer 24 may be anodically bonded to the substrate 22 directly or may be anodically bonded to an interlayer that is bonded to the substrate 22. In certain examples, the cutting layer 24 may be bonded to the substrate 22 indirectly via an interlayer (
A drill bit 10 as shown in
For example, anodic bonding has been used to covalently bond glass to a second material such as silicon, metal, or other materials. In this context, anodic bonding can involve positioning a first material 30, such as glass, and a second material 31, such as silicon, in atomic contact through an electrostatic field. The electrostatic field can attract or repel positive and negative charged ions present in the glass as shown in
In using anodic bonding as a mechanism for attaching a thermally stable polycrystalline material cutting layer to a substrate for use in a drill bit, the characteristics of the thermally stable polycrystalline material and the substrate (and the interlayer, if included) should be considered.
For example, a factor in selecting the thermally stable polycrystalline material, the substrate, and the interlayer (or interlayers) can be the coefficient of thermal expansion (CTE) of each. CTE is the fractional increase in the length per unit rise in temperature for a material. The differential in CTE between the substrate and the thermally stable polycrystalline material may result in thermal residual stress, which can cause the thermally stable polycrystalline material to crack upon being cooled. To minimize problems caused by thermal residual stress, the CTE of the thermally stable polycrystalline material may be similar to that of the substrate or to the interlayer if an interlayer is used.
A glass or alkali or alkaline can be added to the thermally stable polycrystalline material (which does not typically contain glass or such ions) either during the pressing process or post pressing to facilitate anodic bonding to a substrate. For example, typical crystallization Group VIII metal catalysts, such as cobalt and nickel, can be replaced with a carbonate catalyst. Carbonate catalysts can provide the ions utilized for anodic bonding. Examples of such carbonate catalysts include magnesium carbonate (MgCO3), silicon carbonate (SiCO), sodium carbonate (Na2CO3), potassium carbonate (K2CO3), strontium carbonate (SrCO3), calcium carbonate (Ca2CO3), and lithium carbonate (Li2CO3). In some examples, multiple carbonate catalysts are used to form the thermally stable polycrystalline material. Unlike metal catalysts, carbonate catalysts do not function as a catalyst after the press cycle in forming the polycrystalline material. Thus, removal of the carbonate catalyst from the polycrystalline material (for example, by leaching) to generate a fully thermally stable polycrystalline material is not necessary. As shown in
In some examples, the substrate may be covalently coated with a layer of silicon to facilitate the anodic bonding process. As shown in
Heating the thermally stable polycrystalline material and the substrate (or interlayer), as the electrical current is being delivered to the thermally stable polycrystalline material and the substrate, can facilitate the movement of ions to improve anodic bonding. The temperature at which the anodic bonding process occurs influences the amount of time it will take for the bonding to occur. At cooler temperatures, the bonding process may proceed slowly, while at warmer temperatures, the bonding process may occur more quickly. Another factor in selecting the bonding temperature is the temperature at which the bonds of the thermally stable polycrystalline layer degrade. The lower the temperature at which bonding occurs, the lower the residual stress may be in the bonding layer due to geometric changes from the coefficient of thermal expansion (CTE). For example, a thermally stable polycrystalline diamond material can have a maximum temperature limit of approximately 800-1200° C. (depending on atmospheric conditions) at which the diamond bonds begin to break down in the thermally stable polycrystalline material. Thus, in some cases, the temperature selected for the anodic bonding process is as warm as the thermally stable polycrystalline material can be heated with minimal or no degradation. In some examples, the temperature selected for the anodic bonding process may be below the temperature at which the bonds of the thermally stable polycrystalline layer degrade but high enough to increase the rate at which the anodic bonding process occurs. In some examples, the anodic bonding process can involve using relatively low temperatures for bonding. Another factor that can increase the rate of the anodic bonding process is the strength of the electrostatic field. For example, the strength of the electrostatic field can be increased to encourage movement of ions. Increasing the strength of the electrostatic field may also cause the thermally stable polycrystalline material and the substrate (or interlayer) to heat.
In some cases, the temperature for the anodic bonding process may be much lower than the temperature used to debond the joint. For example, for a polycrystalline diamond material, an anodic bond may be created, as the electrical current is being delivered to the thermally stable polycrystalline material and the substrate, at a temperature below 800° C. In some instances, however, the polycrystalline diamond material may be heated to a temperature at or above 800° C. to debond. In some instances, the anodic bonding temperatures, as the electrical current is being delivered to the thermally stable polycrystalline material and the substrate, can be increased, for example, to about 1,000° C., to increase mobility of ions in the thermally stable polycrystalline material and the substrate. The anodic bonding process may be performed such that the thermally stable polycrystalline material is heated, as the electrical current is being delivered to the thermally stable polycrystalline material and the substrate, to a temperature between about 100° C. and about 900° C., or between about 200° C. and about 800° C., or between about 200° C. and about 700° C., or between about 200° C. and about 600° C., or between about 400° C. and about 800° C., or between about 400° C. and about 700° C., or between about 400° C. and about 600° C. For example, the thermally stable polycrystalline material may be heated, as the electrical current is being delivered to the thermally stable polycrystalline material and the substrate, to at least about 100° C., about 200° C., about 300° C., about 400° C., about 500° C., about 600° C., about 700° C., or about 800° C.
In some instances, a heating element is used to for apply heat to the cutting layer (thermally stable polycrystalline material), the substrate (or interlayer), or both the cutting layer and the substrate (or interlayer), to facilitate anodic bonding. In certain examples, the cathode 32 and anode 33 may directly provide heat to the cutting layer and the substrate (or interlayer) as a result of generating an electrostatic field. Alternatively, the anodic bonding process may be performed in an enclosed compartment for heating (for example, a furnace).
To facilitate positioning of the cutting layer and the substrate between them, at least one of the anode and the cathode can be in a fixed position while the other is moveable. The anode and the cathode may both moveable. Positioning the components of the system may be performed manually or robotically using an assembly system. The system may include one or more sensors to facilitate positioning of the various components (not shown). In block 63, an electrical current is delivered to the anode once the cutting layer and the substrate are positioned between the anode and the cathode.
In some examples, the method further includes heating the cutting layer or the substrate when the electrical current is being delivered to the anode 33. In certain examples, the anode 33, the cathode 32, or both, include a heating element. In some cases, the anode 33, the cathode 32, or both, act as a heating element that heat the thermally stable polycrystalline material when the electrical current is delivered to the anode 33. See, for example,
The features described herein may provide a cutting element or hardfacing component with improved wear according to one or more of the following examples.
Example 1: A component includes a cutting layer of a substrate and a thermally stable polycrystalline material anodically bonded to the substrate.
Example 2: The component of Example 1 can feature thermally stable polycrystalline material comprising polycrystalline diamond, or cubic boron nitride.
Example 3: The component of any of Examples 1 to 2 can feature thermally stable polycrystalline material comprising a carbonate.
Example 4: The component of any of Examples 1 to 3 can feature a carbonate comprising at least one of magnesium carbonate, silicon carbonate, sodium carbonate, potassium carbonate, strontium carbonate, calcium carbonate, or lithium carbonate.
Example 5: The component of any of Examples 1 to 4 can feature substrate comprising a carbide or a metal.
Example 6: The component of any of Examples 1 to 5 can feature a carbide substrate comprising cemented tungsten carbide or silicon carbide.
Example 7: The component of any of Examples 1 to 6 can feature a metal substrate comprising steel, a nickel/iron alloy, Invar, or titanium.
Example 8: The component of any of Examples 1 to 7 can feature a metal substrate comprising nickel or cobalt.
Example 9: The component of any of Examples 1 to 8 can feature carbide substrate or metal substrate comprising silicon, or comprising carbide or metal that are covalently coated with silicon.
Example 10: The component of any of Examples 1 to 9 can feature a cutting layer that is bonded to the substrate indirectly via an interlayer.
Example 11: The component of any of Examples 1 to 10 can feature a cutting layer that is anodically bonded to the interlayer, wherein the interlayer is bonded to the substrate.
Example 12: The component of any of Examples 1 to 11 can feature an interlayer comprising a metal.
Example 13: The component of any of Examples 1 to 12 can feature a metal interlayer comprising steel, a nickel/iron alloy, Invar, or titanium.
Example 14: The component of any of Examples 1 to 13 can feature a metal interlayer comprising a metal that is covalently coated with silicon.
Example 15: The component of any of Examples 1 to 14 can be a cutting element, a gage protector, an impact arrestor, or other abrasive or wear-resistant hardfacing component.
Example 16: The component of any of Examples 1 to 15 can be attached to a drill bit, a stabilizer, or a reamer.
Example 17: A system for making the component of any of Example 1 to 16, such as for making a component, includes an anode, a cathode, the substrate in contact with the thermally stable polycrystalline material, and a current generator for sending a current from the anode to the cathode. The thermally stable polycrystalline material and the substrate are disposed between the anode and the cathode. The anode is in contact with the thermally stable polycrystalline material and the cathode is in contact with the substrate. The current generates an electric field and causes anodic bonding between the thermally stable polycrystalline material and the substrate.
Example 18: The system of Example 16 can include a heating element that includes an enclosed compartment for heating and into which the anode, the cathode, the substrate, and the thermally stable polycrystalline material are placed.
Example 19: The system of Example 16 can include a heating element that includes one or more heating element components in contact with at least one of the anode, the cathode, the substrate, or the thermally stable polycrystalline material.
Example 20: A method of making the component according to any of Examples 1 to 16 includes positioning the thermally stable polycrystalline material in contact with a substrate and positioning the thermally stable polycrystalline material and the substrate between an anode and a cathode. The thermally stable polycrystalline material is in contact with the anode, and the substrate is in contact with the cathode. An electrical current is delivered to the anode to generate an electrical field between the anode and the cathode. The electrical field causes the thermally stable polycrystalline material to be anodically bonded to the substrate.
The foregoing description of certain embodiments and features, including illustrated embodiments, has been presented only for the purpose of illustration and description and is not intended to be exhaustive or to limit the disclosure to the precise forms disclosed. Numerous modifications, adaptations, and uses thereof will be apparent to those skilled in the art without departing from the scope of the disclosure. Certain features that are described in this specification in the context of separate embodiments can also be implemented in combination in a single implementation. Conversely, various features that are described in the context of a single implementation can also be implemented in multiple ways separately or in any suitable subcombination. Moreover, although features may be described above as acting in certain combinations, one or more features from a combination can in some cases be excised from the combination, and the combination may be directed to a subcombination or variation of a subcombination. Thus, particular embodiments have been described. Other embodiments are within the scope of the disclosure.
Filing Document | Filing Date | Country | Kind |
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PCT/US2014/055047 | 9/11/2014 | WO | 00 |
Number | Date | Country | |
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61876260 | Sep 2013 | US |