FABRICATION OF DOWNHOLE DRILLING TOOLS
20220250989 · 2022-08-11
Inventors
- Guodong Zhan (Dhahran, SA)
- Jianhui Xu (Dhahran, SA)
- Duanwei He (Chengdu, CN)
- Abrar Alshaikh (Saihat, SA)
Cpc classification
C04B2235/604
CHEMISTRY; METALLURGY
C04B35/528
CHEMISTRY; METALLURGY
C04B2235/66
CHEMISTRY; METALLURGY
C04B2235/785
CHEMISTRY; METALLURGY
C04B2235/786
CHEMISTRY; METALLURGY
C04B2235/5436
CHEMISTRY; METALLURGY
C04B2235/80
CHEMISTRY; METALLURGY
C04B35/5831
CHEMISTRY; METALLURGY
International classification
C04B35/5831
CHEMISTRY; METALLURGY
Abstract
A method of forming a composite cutter for a downhole drilling tool is described. The method includes: mixing a polycrystalline diamond powder and a cubic boron nitride powder with a molar ratio between 0.1 and 0.9 to form a catalyst-free composite mixture; placing the catalyst-free composite mixture into a mold configured in a shape of a cutter; exposing the catalyst-free composite mixture to an ultra-high-pressure, high-temperature treatment including a pressure between 11 Gigapascals (GPa) and 20 GPa, and a temperature between 1300 Kelvins (K) and 2600 K to form a solid composite body; and cooling the solid composite body to form the composite cutter.
Claims
1. A method of forming a composite cutter for a downhole drilling tool, the method comprising: mixing a polycrystalline diamond powder and a cubic boron nitride powder with a molar ratio between 0.1 and 0.9 to form a catalyst-free composite mixture; placing the catalyst-free composite mixture into a mold configured in a shape of a cutter; exposing the catalyst-free composite mixture to an ultra-high-pressure, high-temperature treatment comprising a pressure between 11 Gigapascals (GPa) and 20 GPa, and a temperature between 1300 Kelvins (K) and 2600 K to form a solid composite body; and cooling the solid composite body to form the composite cutter.
2. The method of claim 1, wherein providing the catalyst-free synthesized composite mixture comprises the polycrystalline diamond powder and the cubic boron nitride powder with a characteristic grain size between 0.1 and 50 μm.
3. The method of claim 1, further comprising drying the catalyst-free synthesized composite mixture in a vacuum furnace at a temperature between 1100 K and 1350 K for a duration between 1 hour and 2 hours.
4. The method of claim 1, wherein the ultra-high-pressure, high-temperature treatment comprises between 1 minute and 10 minutes.
5. The method of claim 1, wherein cooling the solid composite body includes between 2 and 10 hours of decompression.
6. The method of claim 1, wherein sintering comprises forming a strong covalent bonding using the cubic boron nitride powder.
7. The method of claim 6, wherein the cubic boron nitride powder acts as a binder.
8. The method of claim 1, further comprises forming new chemical bonds at or near the diamond and cBN grain boundaries of the diamond-cBN composite.
9. The method of claim 8, wherein forming the new chemical bonds include B—C and C—N.
10. The method of claim 1, wherein the drilling tool comprises a PDC drill bit, a reamer, a hole opener, a milling tool, or a stabilizer.
11. A method of forming a composite cutter for a downhole drill tool, the method comprising: mixing a polycrystalline diamond powder and a cubic boron nitride powder with a molar ratio between 0.1 and 0.9 to form a catalyst-free composite mixture; pressing the catalyst-free composite mixture into a mold configured in a shape of a cutter; determining a pressure and a temperature window at which an ultra-high-pressure, high-temperature treatment of the catalyst-free composite mixture forms a solid composite body; exposing the catalyst-free composite mixture to the ultra-high-pressure, high-temperature treatment within the pressure and the temperature window to form the solid composite body; and cooling the solid composite body to form the composite cutter.
12. The method of claim 11, wherein providing the catalyst-free synthesized composite mixture comprises the polycrystalline diamond powder and the cubic boron nitride powder with a characteristic grain size between 0.1 and 50 μm.
13. The method of claim 11, further comprising drying the catalyst-free synthesized composite mixture in a vacuum furnace at a temperature between 1100 K and 1350 K for a duration between 1 hour and 2 hours.
14. The method of claim 11, wherein the ultra-high-pressure, high-temperature treatment comprises between 1 minute and 10 minutes.
15. The method of claim 11, wherein cooling the solid composite body includes between 2 and 10 hours of decompression.
16. The method of claim 11, wherein sintering comprises forming a strong covalent bonding using the cubic boron nitride powder.
17. The method of claim 16, wherein the cubic boron nitride powder acts as a binder.
18. The method of claim 11, further comprises forming new chemical bonds at or near the diamond and cBN grain boundaries of the diamond-cBN composite.
19. The method of claim 18, wherein forming the new chemical bonds include B—C and C—N.
20. The method of claim 11, wherein the drilling tool comprises a PDC drill bit, a reamer, a hole opener, a milling tool, or a stabilizer.
Description
DESCRIPTION OF DRAWINGS
[0017]
[0018]
[0019]
[0020]
[0021]
[0022]
[0023]
DETAILED DESCRIPTION
[0024] This specification describes a method for fabricating catalyst-free ultrahard composite cutters that can be used to extend the life of PDC drilling tools. The drilling tools include PDC drill bits, reamers, hole openers, milling tools, and stabilizers. The models and methods described in this specification provide a mechanical alloying procedure to fabricate a composite cutter. The PDC drill bits with the composite cutters can be used to improve drilling efficiency in oil and gas wellbore formations.
[0025] A polycrystalline diamond powder and a cubic boron nitride powder with a characteristic grain size between 0.1 and 50 micrometers (μall) are mechanically mixed to form a composite mixture. The composite mixture is placed in a mold with a shape of a cutter and an ultra-high-pressure, high-temperature treatment (UHPHT) is applied. The sintering treatment initiates a solid phase reaction within the composite mixture as a result of applied pressure between 11 gigapascal (GPa) and 20 GPa, and applied temperature between 1300 Kelvins (K) and 2600 K. The solid phase reaction includes formation of new chemical bonds (e.g., boron-carbon (B—C) and carbon-nitrogen (C—N)) at or near the diamond and cBN grain boundaries of the diamond-cBN composite. After the UHPHT treatment is terminated, the composite mixture is cooled down and decompressed for up to 15 hours. The final composite mixture has a shape of a composite cutter ready to be assembled into a drill bit and drill highly abrasive oil and gas formations.
[0026]
[0027]
[0028]
[0029] The UHPHT treatment includes forming a solid composite cutter using compressive pressure between 11 GPa and 20 GPa, and temperature between 1300 Kelvins (K) and 2600 K. Further details of this UHPHT process are described in U.S. patent application Ser. No. 16/524,935 filed on Jul. 29, 2019, U.S. Patent Application No. 63/031,077 filed on May 28, 2020, and U.S. Patent Application No. 63/033,669 filed on Jun. 2, 2020, and the entire content is incorporated here by reference. The composite cutter 144 can be formed using a two-stage, multi-anvil cubic press system (e.g., the 6-8type, DS6×25 MN cubic press machine produced by Chengdu Dongwei Science and Technology Company of 2039 South Section of Tianfu Avenue, Tianfu New District, Chengdu 610213, Sichuan Province, P. R. China.)
[0030]
[0031]
[0032] The cavity 184 is filled with a composite mixture including the polycrystalline diamond powder and the cubic boron nitride powder. In some implementations, the powders may have particle sizes up to 50 μm. In some implementations, the powders may have particle sizes down to 0.1 μm. In some implementations, the powders may have a grain or particle size of between 8 micrometers (μm) to 12 μm. The composite mixture is treated in a vacuum furnace at approximately 1300 K (e.g., between 1100 K and 1350 K) for a duration between 1 and 2 hours. For example, a vacuum pressure of between 1×10.sup.−2 and 1×10.sup.−4 Torr can be applied to the composite mixture in the vacuum furnace. At this step, the particles of the mixture are still in a loose granular state during this treatment. In some implementations, the composite mixture is placed in a corundum container, which is introduced into a vacuum furnace. A vacuum is applied to the vacuum furnace until the pressure within the vacuum furnace between 1×10.sup.−2 and 1×10.sup.−4 Torr. The composite mixture is heated at a rate between 1 and 50° C. per minute until a temperature of approximately 1300 K is reached. When the vacuum treatment is complete, the composite mixture is incorporated into a capsule to form a composite cutter.
[0033]
[0034] The capsule 228 is placed in the cavity 184 of the booster 180. A mixture of 99.99% pure MgO doped chromium trioxide (Cr.sub.2O.sub.3), at five percent by weight, is also introduced into the cavity 184 and serves as a pressure transmitting medium. With the cylindrical capsule and the pressure-transmitting medium added to the cavity 184, the booster 180 is enclosed and cemented with the strips 186 disposed between adjacent cubes 182. The booster 180 loaded with composite mixture is placed in between the anvils 172 of the first stage 168 of the cubic press. With the booster 180 in position, the anvils 172 are advanced and engage the booster 180. A central contact surface 208 of each anvil 172 contacts an adjacent exterior surface of the booster 180. Consequently, as loading is applied to the booster 180 by the anvils 172, the anvils 172 apply loads in six directions on the outer six surfaces of the booster 180. The loading applied by the anvils 172 pushes the cubes 182 towards each other, compressing the pressure-transmitting medium, thereby generating large pressures within the cavity 184. As the anvils 172 are advanced, the booster 180 deforms such that WC—Co material forming the cubes 182 is displaced into the gaps formed between adjacent anvils 172 at adjacent chamfered edges 208. As a result, this displaced WC—Co material forms sealing edges between the adjacent anvils 172. In some cases, the sealing material is pyrophyllite that is squeezing out to fill the gaps of the anvils to prevent the anvils from directly contacting each other. The central contact surfaces 208 and the sealed edges combine to form a two-stage pressure chamber. As loading is applied to the booster 180, the strips 186 placed between the cubes 182 and the pressure-transmitting medium are squeezed and flow to form a sealing edge between the adjacent cubes 182. Using this two-stage system, cutters with a variety of compositions and shapes can be fabricated.
[0035]
[0036] UHPHT cutter production methods encompassed by the present disclosure may take from eight hours to twelve hours to complete. Also, although the example method 276 describes a maximum pressure applied to the sample of 20 GPa, the UHPHT methods encompass ultra-high pressures within a range of 10 GPa to 35 GPa. More generally, ultra-high pressures of a UHPHT method are greater than pressures used in current HPHT methods. Current HPHT methods involve pressures within a range of 5.5 GPa and 7 GPa. Thus, pressures in excess of those used in current HPHT methods are UHPHT pressures within the scope of the present disclosure. Although an upper range of 35 GPa is indicated, in other implementations, UHPHT methods within the scope of the present disclosure may use pressures that exceed 35 GPa.
[0037] With the UHPHT method complete, the sample is extracted, such as from a cubic press. In some implementations, the sample is subjected to an acid treatment to remove the one or more components included with the composite mixture. For example, where the composite mixture is incorporated into a capsule, such as a capsule 228 described earlier, the capsule is subjected to an acid treatment to remove tantalum foil. In some implementations, the sample is washed in water, followed by a wash in ethanol using an ultrasonic bath. The ultrasonic bath was used in washing with water first and then ethanol.
[0038] While this specification contains many specific implementation details, these should not be construed as limitations on the scope of what may be claimed, but rather as descriptions of features that may be specific to particular implementations. Certain features that are described in this specification in the context of separate implementations 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 implementations, separately, or any suitable sub-combination. Moreover, although previously described features may be described as acting in certain combinations and even initially claimed as such, one or more features from a claimed combination can, in some cases, be excised from the combination, and the claimed combination may be directed to a sub-combination or variation of a sub-combination.
[0039] Particular implementations of the subject matter have been described. Other implementations, alterations, and permutations of the described implementations are within the scope of the following claims as will be apparent to those skilled in the art. While operations are depicted in the drawings or claims in a particular order, this should not be understood as requiring that such operations be performed in the particular order shown or in sequential order, or that all illustrated operations be performed (some operations may be considered optional), to achieve desirable results. In certain circumstances, multitasking or parallel processing (or a combination of multitasking and parallel processing) may be advantageous and performed as deemed appropriate.
[0040] Accordingly, the previously described example implementations do not define or constrain the present disclosure. Other changes, substitutions, and alterations are also possible without departing from the spirit and scope of the present disclosure.
[0041] A number of embodiments of these systems and methods have been described. Nevertheless, it will be understood that various modifications may be made without departing from the spirit and scope of this disclosure. Accordingly, other embodiments are within the scope of the following claims.