CN113234982A - Preparation method of PDC drill bit matrix material - Google Patents

Preparation method of PDC drill bit matrix material Download PDF

Info

Publication number
CN113234982A
CN113234982A CN202110431964.1A CN202110431964A CN113234982A CN 113234982 A CN113234982 A CN 113234982A CN 202110431964 A CN202110431964 A CN 202110431964A CN 113234982 A CN113234982 A CN 113234982A
Authority
CN
China
Prior art keywords
tungsten carbide
alloy
entropy alloy
framework material
powder
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Granted
Application number
CN202110431964.1A
Other languages
Chinese (zh)
Other versions
CN113234982B (en
Inventor
郭智兴
高栗寒
林霜岚
华涛
熊计
荆凯峰
鲜广
杨天恩
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Sichuan University
Original Assignee
Sichuan University
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Sichuan University filed Critical Sichuan University
Priority to CN202110431964.1A priority Critical patent/CN113234982B/en
Publication of CN113234982A publication Critical patent/CN113234982A/en
Application granted granted Critical
Publication of CN113234982B publication Critical patent/CN113234982B/en
Active legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Images

Classifications

    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22CALLOYS
    • C22C29/00Alloys based on carbides, oxides, nitrides, borides, or silicides, e.g. cermets, or other metal compounds, e.g. oxynitrides, sulfides
    • C22C29/02Alloys based on carbides, oxides, nitrides, borides, or silicides, e.g. cermets, or other metal compounds, e.g. oxynitrides, sulfides based on carbides or carbonitrides
    • C22C29/06Alloys based on carbides, oxides, nitrides, borides, or silicides, e.g. cermets, or other metal compounds, e.g. oxynitrides, sulfides based on carbides or carbonitrides based on carbides, but not containing other metal compounds
    • C22C29/08Alloys based on carbides, oxides, nitrides, borides, or silicides, e.g. cermets, or other metal compounds, e.g. oxynitrides, sulfides based on carbides or carbonitrides based on carbides, but not containing other metal compounds based on tungsten carbide
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B22CASTING; POWDER METALLURGY
    • B22FWORKING METALLIC POWDER; MANUFACTURE OF ARTICLES FROM METALLIC POWDER; MAKING METALLIC POWDER; APPARATUS OR DEVICES SPECIALLY ADAPTED FOR METALLIC POWDER
    • B22F9/00Making metallic powder or suspensions thereof
    • B22F9/02Making metallic powder or suspensions thereof using physical processes
    • B22F9/04Making metallic powder or suspensions thereof using physical processes starting from solid material, e.g. by crushing, grinding or milling
    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22CALLOYS
    • C22C1/00Making non-ferrous alloys
    • C22C1/10Alloys containing non-metals
    • C22C1/1036Alloys containing non-metals starting from a melt
    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22CALLOYS
    • C22C1/00Making non-ferrous alloys
    • C22C1/10Alloys containing non-metals
    • C22C1/1036Alloys containing non-metals starting from a melt
    • C22C1/1057Reactive infiltration
    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22CALLOYS
    • C22C29/00Alloys based on carbides, oxides, nitrides, borides, or silicides, e.g. cermets, or other metal compounds, e.g. oxynitrides, sulfides
    • C22C29/02Alloys based on carbides, oxides, nitrides, borides, or silicides, e.g. cermets, or other metal compounds, e.g. oxynitrides, sulfides based on carbides or carbonitrides
    • C22C29/06Alloys based on carbides, oxides, nitrides, borides, or silicides, e.g. cermets, or other metal compounds, e.g. oxynitrides, sulfides based on carbides or carbonitrides based on carbides, but not containing other metal compounds
    • C22C29/067Alloys based on carbides, oxides, nitrides, borides, or silicides, e.g. cermets, or other metal compounds, e.g. oxynitrides, sulfides based on carbides or carbonitrides based on carbides, but not containing other metal compounds comprising a particular metallic binder
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B22CASTING; POWDER METALLURGY
    • B22FWORKING METALLIC POWDER; MANUFACTURE OF ARTICLES FROM METALLIC POWDER; MAKING METALLIC POWDER; APPARATUS OR DEVICES SPECIALLY ADAPTED FOR METALLIC POWDER
    • B22F9/00Making metallic powder or suspensions thereof
    • B22F9/02Making metallic powder or suspensions thereof using physical processes
    • B22F9/04Making metallic powder or suspensions thereof using physical processes starting from solid material, e.g. by crushing, grinding or milling
    • B22F2009/043Making metallic powder or suspensions thereof using physical processes starting from solid material, e.g. by crushing, grinding or milling by ball milling

Landscapes

  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Mechanical Engineering (AREA)
  • Metallurgy (AREA)
  • Organic Chemistry (AREA)
  • Manufacture Of Alloys Or Alloy Compounds (AREA)
  • Powder Metallurgy (AREA)

Abstract

The invention discloses a preparation method of a PDC drill bit matrix material, which is characterized in that high-entropy alloy with a face-centered cubic and body-centered cubic eutectic structure is added into cast tungsten carbide and single-crystal tungsten carbide powder, agarose sol is added after mixing to form slurry, then the slurry is injected into a mold and dried to form the slurry, and finally copper-based dipping alloy is added to carry out infiltration in a vacuum furnace to form the PDC drill bit matrix material containing the high-entropy alloy with the face-centered cubic and body-centered cubic eutectic structures which are uniformly distributed. The preparation method solves the problems that tungsten carbide and metal additives existing in the existing preparation method of the PDC drill bit matrix material are difficult to uniformly disperse, and the like, the hardness is more than or equal to 30HRC, the bending strength is more than or equal to 600MPa, the impact toughness is more than or equal to 4J, and the comprehensive mechanical property is excellent.

Description

Preparation method of PDC drill bit matrix material
Technical Field
The invention relates to a preparation method of a matrix material, in particular to a preparation method of a PDC drill bit matrix material, and belongs to the field of composite materials.
Background
The use of PDC (diamond compact) drill bits is becoming increasingly common in oil production. The PDC drill bit is composed of PDC cutting teeth and a matrix material, the PDC cutting teeth are embedded in the matrix, and the comprehensive performances of hardness, wear resistance, strength, toughness and the like of the matrix are very important for the use performance of the PDC drill bit. The academic and industrial circles pay great attention to the research on the matrix material and the preparation method thereof. CN201911079586.4 discloses a drill bit matrix material and a preparation method thereof, and the components of the material comprise 45.0-65.0% of tungsten carbide hard particles and 35.0-55.0% of copper-containing multi-principal element high-entropy alloy. The preparation method of the drill bit matrix material comprises the steps of carrying out die filling and compaction on tungsten carbide hard particles, and then infiltrating copper-containing multi-principal-element high-entropy alloy at high temperature to obtain the drill bit matrix material, wherein the wear resistance, the strength and the impact toughness of the drill bit matrix material can be greatly improved, so that the service life of the matrix drill bit can be remarkably prolonged, and the drill bit matrix material is particularly suitable for drilling of medium-hard strata. The bonding metal nickel powder is also added into the tungsten carbide cast by the matrix material framework powder, when the nickel content is 2 percent, the performance is in the best state, the bending strength reaches 960MPa, and the impact toughness reaches 3.62J/cm2(Weshifai et al. influence of nickel content on performance of infiltrated matrix material. protective engineering. 2 nd 2019). However, the existing preparation method of the carcass material has two problems: firstly, the added metal powder is difficult to be uniformly dispersed around the carbide hard phase by adopting a tap mode; secondly, although the performance of the matrix material can be improved by carrying out high entropy melting on the copper alloy for dipping the alloy, after the high entropy copper alloy is melted at high temperature in the infiltration process, low melting point metal in the high entropy copper alloy is easy to lose, and the high entropy alloy can have structural relaxation, so that the phase structure of the high entropy alloy is difficult to maintain, and the performance advantage of the high entropy alloy is difficult to be exerted. Therefore, a method for preparing a high-performance carcass material still needs to be continuously developed.
Disclosure of Invention
Aiming at the problems of the existing matrix material preparation method, the invention provides a PDC drill bit matrix material containing uniformly distributed face-centered cubic and body-centered cubic phase eutectic structure high-entropy alloy, which is prepared by adding the high-entropy alloy with the face-centered cubic and body-centered cubic phase eutectic structures into cast tungsten carbide and single-crystal tungsten carbide powder, mixing, adding agarose sol to form slurry, injecting the slurry into a mold, drying and molding, and finally adding copper-based dipping alloy to perform infiltration in a vacuum furnace.
The preparation method of the PDC drill bit matrix material is characterized by sequentially comprising the following steps of:
(1) preparing framework material powder containing high-entropy alloy: preparing framework material powder from cast tungsten carbide, single crystal tungsten carbide powder and AlCoCrFeNiCu high-entropy alloy powder, wherein the AlCoCrFeNiCu is a face-centered cubic and body-centered cubic eutectic structure, the proportion of the AlCoCrFeNiCu in the mixed powder is 2-6 wt.%, the single crystal tungsten carbide accounts for 20-60 wt.%, and the balance is cast tungsten carbide; putting the skeleton powder into a planetary ball mill for dry mixing for 2-4 h to prepare skeleton material powder containing the high-entropy alloy;
(2) preparing agarose sol: adding agarose into deionized water to prepare a solution of 1-5 wt.%, putting the solution into a constant-temperature water bath kettle, preserving heat for 2-3 hours at 80-90 ℃, stirring in the heat preservation process to form agarose sol, and keeping the temperature of the agarose sol at 50-60 ℃ after heat preservation;
(3) preparing framework material slurry: adding agarose sol into skeleton material powder containing high-entropy alloy, wherein the skeleton material powder accounts for 30-40 wt%, preserving heat at 50-60 ℃ for 30-40 min, stirring in the heat preservation process, and forming skeleton material slurry after heat preservation;
(4) molding a framework material blank: pouring the framework material slurry into a graphite mold, and drying in a vacuum drying oven at 100-110 ℃ for 1-2 h to form a framework material blank, wherein the cast tungsten carbide, the single crystal tungsten carbide and the high-entropy alloy are uniformly distributed in the blank;
(5) preparing a PDC drill bit matrix material: placing Cu-Ni-Mn-Sn alloy particles on the upper part of the framework material blank, wherein the weight ratio of the Cu-Ni-Mn-Sn alloy particles to the framework material blank is 1: 1-1.3: 1; then putting the framework material blank body in which the Cu-Ni-Mn-Sn alloy is placed and a graphite mould into a vacuum sintering furnace, keeping the temperature at 400-600 ℃ for 1-2 h to decompose and remove agarose, keeping the temperature at 1150-1200 ℃ for 1-2 h to melt the Cu-Ni-Mn-Sn alloy and immerse the Cu-Ni-Mn-Sn alloy into the framework material blank body, filling pores among cast tungsten carbide, single crystal tungsten carbide and high-entropy alloy and pores left after the agarose is removed, introducing Ar gas with the flow rate of 5-10L/h to rapidly cool after the heat preservation is finished, avoiding the structural relaxation of the high-entropy alloy, keeping the eutectic cubic and body-centered cubic phase structures of the AlCoCrFeNiCu high-entropy alloy, and enabling the tungsten carbide to have no solid solution in the high-entropy alloy, thereby preparing the PDC drill bit matrix material containing the face-centered cubic and body-centered cubic phase eutectic structure high-entropy alloy phases, the hardness is more than or equal to 30HRC, the bending strength is more than or equal to 600MPa, and the impact toughness is more than or equal to 4J.
The preparation method of the PDC drill bit matrix material is further characterized by comprising the following steps:
(1) when the skeleton powder is mixed in a planetary ball mill, the rotating speed of the ball mill is 100-300 r/min;
(2) the stirring speed during the preparation of the agarose sol is 60-100 r/min;
(3) the stirring speed during preparation of the framework material slurry is 60-100 r/min;
(4) when the framework material blank is formed, the drying vacuum degree is less than 20 Pa;
(5) the temperature rise speed during the preparation of the matrix material is 10 ℃/min, the Cu-Ni-Mn-Sn alloy comprises 9.5-11.5 wt% of nickel, 5.5-6.5 wt% of Sn, 5-6.5 wt% of Mn and the balance of Cu.
The invention has the advantages that: (1) the existing tire body preparation method takes high-entropy alloy as an impregnating material, and low-melting-point alloy is easy to run off after being melted and is difficult to maintain the phase structure of the high-entropy alloy; the high-entropy alloy is added into the framework material and uniformly dispersed, and the face-centered cubic structure and the body-centered cubic eutectic phase structure are maintained after infiltration, so that the strength and the toughness of the matrix material can be improved; (2) in the traditional method, a tap method is adopted, the difference between the granularity, the morphology, the specific gravity and the like of spherical cast tungsten carbide powder and other added metal or alloy powder is large, and the metal powder is difficult to be uniformly dispersed with the tungsten carbide powder in the tap process; in the invention, the skeleton material blank is prepared by adopting a dry ball milling and sol slurry forming mode, so that the high-entropy alloy powder and the tungsten carbide powder can be uniformly mixed, the gap uniformity among particles is higher, and the alloy after infiltration is more uniform. (3) The high-entropy alloy adopted in the invention has a delayed diffusion effect, and cannot dissolve in a tungsten carbide metal phase when metals such as nickel and the like are added, so that the content, volume fraction and morphology of tungsten carbide particles are maintained.
Drawings
FIG. 1 is a schematic diagram of a method for preparing a PDC bit matrix material of the present invention.
Detailed Description
Example 1: preparing PDC drill bit matrix material according to the following steps
(1) Preparing framework material powder containing high-entropy alloy: preparing framework material powder from cast tungsten carbide, single crystal tungsten carbide powder and AlCoCrFeNiCu high-entropy alloy powder, wherein AlCoCrFeNiCu is a face-centered cubic and body-centered cubic eutectic structure, the ratio of the AlCoCrFeNiCu in the mixed powder is 3wt.%, the single crystal tungsten carbide is 32wt.%, and the balance is cast tungsten carbide; putting the skeleton powder into a planetary ball mill for dry mixing for 4 hours, wherein the rotating speed of the ball mill is 150r/min, so that skeleton material powder containing the high-entropy alloy is prepared;
(2) preparing agarose sol: adding agarose into deionized water to prepare a 2wt.% solution, placing the solution into a constant-temperature water bath kettle, preserving heat for 2 hours at 85 ℃, stirring the solution at the stirring speed of 80r/min during the heat preservation process to form agarose sol, and keeping the temperature of the agarose sol at 52 ℃ after the heat preservation;
(3) preparing framework material slurry: adding agarose sol into skeleton material powder containing high-entropy alloy, wherein the skeleton material powder accounts for 30 wt%, preserving heat at 55 ℃ for 30min, stirring at the stirring speed of 70r/min during the heat preservation process, and forming skeleton material slurry after the heat preservation is finished;
(4) molding a framework material blank: pouring the framework material slurry into a graphite mold, drying for 1h in a vacuum drying oven at 100 ℃ and the drying vacuum degree of 19Pa to form a framework material blank, wherein the cast tungsten carbide, the single crystal tungsten carbide and the high-entropy alloy are uniformly distributed in the blank;
(5) preparing a PDC drill bit matrix material: placing Cu-Ni-Mn-Sn alloy particles on the upper part of a framework material blank, wherein the Cu-Ni-Mn-Sn alloy comprises the components of 10wt.% of nickel, 5.5wt.% of Sn, 5.5wt.% of Mn and the balance of Cu; the weight ratio of the Cu-Ni-Mn-Sn alloy particles to the framework material blank is 1: 1; then putting the framework material blank body in which the Cu-Ni-Mn-Sn alloy is placed and a graphite mold into a vacuum sintering furnace together, wherein the initial vacuum degree is 18Pa, the heating speed is 10 ℃/min, and the temperature is kept at 450 ℃ for 1h to decompose and remove the agarose; heating to 1150 ℃ at the speed of 10 ℃/min, preserving heat for 1h to melt Cu-Ni-Mn-Sn alloy, immersing the Cu-Ni-Mn-Sn alloy into a framework material blank, filling pores among cast tungsten carbide, monocrystal tungsten carbide and high-entropy alloy and pores left after agarose is removed, introducing Ar gas with the flow of 6L/h to rapidly cool after heat preservation is finished, avoiding structural relaxation of the high-entropy alloy, keeping a face-centered cubic and body-centered cubic eutectic structure of the AlCoCrFeNiCu high-entropy alloy, and preparing the PDC drill bit matrix material containing the high-entropy alloy phase with the face-centered cubic and body-centered cubic eutectic structures, wherein the hardness of the PDC drill bit matrix material is 31HRC, the bending strength of the PDC drill bit matrix material is 650MPa, and the impact toughness of the PDC drill bit matrix material is 4J.
Example 2: preparing PDC drill bit matrix material according to the following steps
(1) Preparing framework material powder containing high-entropy alloy: preparing framework material powder from cast tungsten carbide, single crystal tungsten carbide powder and AlCoCrFeNiCu high-entropy alloy powder, wherein the AlCoCrFeNiCu is a face-centered cubic and body-centered cubic eutectic structure, the proportion of the AlCoCrFeNiCu in the mixed powder is 4wt.%, the single crystal tungsten carbide is 45wt.%, and the balance is cast tungsten carbide; putting the skeleton powder into a planetary ball mill for dry mixing for 3 hours, wherein the rotating speed of the ball mill is 250r/min, so that skeleton material powder containing high-entropy alloy is prepared;
(2) preparing agarose sol: adding agarose into deionized water to prepare a 4wt.% solution, placing the solution into a constant-temperature water bath kettle, preserving heat for 3 hours at 90 ℃, stirring the solution during the heat preservation process at a stirring speed of 90r/min to form agarose sol, and keeping the temperature of the agarose sol at 60 ℃ after the heat preservation;
(3) preparing framework material slurry: adding agarose sol into framework material powder containing high-entropy alloy, wherein the framework material powder accounts for 40 wt%, preserving heat at 58 ℃ for 40min, stirring at the stirring speed of 80r/min in the heat preservation process, and forming framework material slurry after heat preservation;
(4) molding a framework material blank: pouring the framework material slurry into a graphite mold, drying for 2 hours in a vacuum drying oven at 110 ℃ under the drying vacuum degree of 15Pa to form a framework material blank, wherein the cast tungsten carbide, the single crystal tungsten carbide and the high-entropy alloy are uniformly distributed in the blank;
(5) preparing a PDC drill bit matrix material: placing Cu-Ni-Mn-Sn alloy particles on the upper part of a framework material blank, wherein the Cu-Ni-Mn-Sn alloy comprises the components of 11.5wt.% of nickel, 6.5wt.% of Sn, 6wt.% of Mn and the balance of Cu; the weight ratio of the Cu-Ni-Mn-Sn alloy particles to the framework material blank is 1.2: 1; then putting the framework material blank body in which the Cu-Ni-Mn-Sn alloy is placed and a graphite mold into a vacuum sintering furnace together, wherein the initial vacuum degree is 16Pa, the heating speed is 10 ℃/min, and the temperature is kept at 500 ℃ for 2h to decompose and remove the agarose; heating to 1180 ℃ at the speed of 10 ℃/min, preserving heat for 2 hours to melt and immerse the Cu-Ni-Mn-Sn alloy into a framework material blank, filling pores among cast tungsten carbide, monocrystal tungsten carbide and high-entropy alloy and pores left after agarose is removed, introducing Ar gas with the flow of 8L/h to rapidly cool after heat preservation is finished, avoiding structural relaxation of the high-entropy alloy, keeping a face-centered cubic and body-centered cubic eutectic structure of AlCoCrFeNiCu high-entropy alloy, and preparing the PDC drill bit matrix material containing the high-entropy alloy phase with the face-centered cubic and body-centered cubic eutectic structures, wherein the hardness is 33HRC, the bending strength is more than or equal to 760MPa, and the impact toughness is 5J.

Claims (2)

1. A preparation method of a PDC drill bit matrix material is characterized by sequentially comprising the following steps:
(1) preparing framework material powder containing high-entropy alloy: preparing framework material powder from cast tungsten carbide, single crystal tungsten carbide powder and AlCoCrFeNiCu high-entropy alloy powder, wherein the AlCoCrFeNiCu is a face-centered cubic and body-centered cubic eutectic structure, the proportion of the AlCoCrFeNiCu in the mixed powder is 2-6 wt.%, the single crystal tungsten carbide accounts for 20-60 wt.%, and the balance is cast tungsten carbide; putting the skeleton powder into a planetary ball mill for dry mixing for 2-4 h to prepare skeleton material powder containing the high-entropy alloy;
(2) preparing agarose sol: adding agarose into deionized water to prepare a solution of 1-5 wt.%, putting the solution into a constant-temperature water bath kettle, preserving heat for 2-3 hours at 80-90 ℃, stirring in the heat preservation process to form agarose sol, and keeping the temperature of the agarose sol at 50-60 ℃ after heat preservation;
(3) preparing framework material slurry: adding agarose sol into skeleton material powder containing high-entropy alloy, wherein the skeleton material powder accounts for 30-40 wt%, preserving heat at 50-60 ℃ for 30-40 min, stirring in the heat preservation process, and forming skeleton material slurry after heat preservation;
(4) molding a framework material blank: pouring the framework material slurry into a graphite mold, and drying in a vacuum drying oven at 100-110 ℃ for 1-2 h to form a framework material blank, wherein the cast tungsten carbide, the single crystal tungsten carbide and the high-entropy alloy are uniformly distributed in the blank;
(5) preparing a PDC drill bit matrix material: placing Cu-Ni-Mn-Sn alloy particles on the upper part of the framework material blank, wherein the weight ratio of the Cu-Ni-Mn-Sn alloy particles to the framework material blank is 1: 1-1.3: 1; then putting the framework material blank body in which the Cu-Ni-Mn-Sn alloy is placed and a graphite mould into a vacuum sintering furnace, keeping the temperature at 400-600 ℃ for 1-2 h to decompose and remove agarose, keeping the temperature at 1150-1200 ℃ for 1-2 h to melt the Cu-Ni-Mn-Sn alloy and immerse the Cu-Ni-Mn-Sn alloy into the framework material blank body, filling pores among cast tungsten carbide, single crystal tungsten carbide and high-entropy alloy and pores left after the agarose is removed, introducing Ar gas with the flow rate of 5-10L/h to rapidly cool after the heat preservation is finished, avoiding the structural relaxation of the high-entropy alloy, keeping the eutectic cubic and body-centered cubic phase structures of the AlCoCrFeNiCu high-entropy alloy, and enabling the tungsten carbide to have no solid solution in the high-entropy alloy, thereby preparing the PDC drill bit matrix material containing the face-centered cubic and body-centered cubic phase eutectic structure high-entropy alloy phases, the hardness is more than or equal to 30HRC, the bending strength is more than or equal to 600MPa, and the impact toughness is more than or equal to 4J.
2. The method of preparing a PDC bit matrix material of claim 1, further characterized by:
(1) when the skeleton powder is mixed in a planetary ball mill, the rotating speed of the ball mill is 100-300 r/min;
(2) the stirring speed during the preparation of the agarose sol is 60-100 r/min;
(3) the stirring speed during preparation of the framework material slurry is 60-100 r/min;
(4) when the framework material blank is formed, the drying vacuum degree is less than 20 Pa;
(5) the temperature rise speed during the preparation of the matrix material is 10 ℃/min, the Cu-Ni-Mn-Sn alloy comprises 9.5-11.5 wt% of nickel, 5.5-6.5 wt% of Sn, 5-6.5 wt% of Mn and the balance of Cu.
CN202110431964.1A 2021-04-21 2021-04-21 Preparation method of PDC drill bit matrix material Active CN113234982B (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN202110431964.1A CN113234982B (en) 2021-04-21 2021-04-21 Preparation method of PDC drill bit matrix material

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN202110431964.1A CN113234982B (en) 2021-04-21 2021-04-21 Preparation method of PDC drill bit matrix material

Publications (2)

Publication Number Publication Date
CN113234982A true CN113234982A (en) 2021-08-10
CN113234982B CN113234982B (en) 2022-02-08

Family

ID=77129722

Family Applications (1)

Application Number Title Priority Date Filing Date
CN202110431964.1A Active CN113234982B (en) 2021-04-21 2021-04-21 Preparation method of PDC drill bit matrix material

Country Status (1)

Country Link
CN (1) CN113234982B (en)

Citations (22)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20090074604A1 (en) * 2007-09-19 2009-03-19 Industrial Technology Research Institute Ultra-hard composite material and method for manufacturing the same
CN101670421A (en) * 2009-10-16 2010-03-17 大连理工大学 Methods for preparing copper-plate surface modifying WC-Cu alloy layer for continuous-cast crystallizer and application thereof
CN102146771A (en) * 2010-12-28 2011-08-10 中国石油大学(华东) Hot pressed and diamond impregnated drill tooth applicable to strong abrasive hard formation
CN102489699A (en) * 2011-12-21 2012-06-13 深圳新速通石油工具有限公司 Polycrystalline diamond compact (PDC) drillbit matrix powder and process for manufacturing matrix by using same
CN102796933A (en) * 2012-09-04 2012-11-28 四川大学 High-entropy alloy binder phase-based nitrogen-containing hard alloy and preparation method thereof
CN106077610A (en) * 2016-06-17 2016-11-09 广东省材料与加工研究所 A kind of bit matrix metallurgy powder
CN108060322A (en) * 2017-12-07 2018-05-22 中南大学 The preparation method of hard high-entropy alloy composite material
CN108463301A (en) * 2016-02-29 2018-08-28 山特维克知识产权股份有限公司 Hard alloy containing alternative binder
CN109022995A (en) * 2018-07-26 2018-12-18 铜陵长江金刚石工具有限责任公司 A kind of diamond drill bit matrix and its manufacturing method
CN109023013A (en) * 2018-08-29 2018-12-18 中国科学院兰州化学物理研究所 A kind of preparation method of anti-corrosion and high strength AlCoCrFeNi-Cu high-entropy alloy
CN109112378A (en) * 2018-09-21 2019-01-01 四川煜兴新型材料科技有限公司 A kind of preparation method of new bonding phase cemented carbide material
CN109136711A (en) * 2018-07-27 2019-01-04 天津立林石油机械有限公司 Novel high wear-resistant TC bearing
CN109136601A (en) * 2018-09-10 2019-01-04 南京工程学院 A kind of high hardware heart cubic phase enhances the high-entropy alloy composite material and preparation method of tough modeling face-centred cubic structure
CN109161774A (en) * 2018-11-23 2019-01-08 西安工业大学 Haystellite and preparation method thereof by high-entropy alloy as binder
CN109161773A (en) * 2018-09-21 2019-01-08 成都理工大学 A kind of preparation method of high-entropy alloy bonding phase cemented carbide
CN109252081A (en) * 2018-10-31 2019-01-22 华南理工大学 A kind of high-entropy alloy Binder Phase ultrafine tungsten carbide hard alloy and preparation method thereof
CN109371307A (en) * 2018-11-29 2019-02-22 福建工程学院 It is a kind of using high-entropy alloy powder as the preparation method of the WC base cemented carbide of binder
CN109518057A (en) * 2018-10-11 2019-03-26 东莞理工学院 A kind of tungsten carbide material and its preparation method and application by high-entropy alloy cobalt ferronickel aluminum bronze bonding
CN110643880A (en) * 2019-11-07 2020-01-03 广东省材料与加工研究所 Drill bit matrix material and preparation method thereof
CN110684935A (en) * 2019-11-07 2020-01-14 广东省材料与加工研究所 Drill bit matrix material and preparation method thereof
CN111621661A (en) * 2020-06-09 2020-09-04 山东威尔斯通钨业有限公司 Preparation method of tungsten carbide copper
CN113073274A (en) * 2021-03-31 2021-07-06 湖南大学 Novel method for preparing double-phase ultra-fine grain high-entropy alloy

Patent Citations (22)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20090074604A1 (en) * 2007-09-19 2009-03-19 Industrial Technology Research Institute Ultra-hard composite material and method for manufacturing the same
CN101670421A (en) * 2009-10-16 2010-03-17 大连理工大学 Methods for preparing copper-plate surface modifying WC-Cu alloy layer for continuous-cast crystallizer and application thereof
CN102146771A (en) * 2010-12-28 2011-08-10 中国石油大学(华东) Hot pressed and diamond impregnated drill tooth applicable to strong abrasive hard formation
CN102489699A (en) * 2011-12-21 2012-06-13 深圳新速通石油工具有限公司 Polycrystalline diamond compact (PDC) drillbit matrix powder and process for manufacturing matrix by using same
CN102796933A (en) * 2012-09-04 2012-11-28 四川大学 High-entropy alloy binder phase-based nitrogen-containing hard alloy and preparation method thereof
CN108463301A (en) * 2016-02-29 2018-08-28 山特维克知识产权股份有限公司 Hard alloy containing alternative binder
CN106077610A (en) * 2016-06-17 2016-11-09 广东省材料与加工研究所 A kind of bit matrix metallurgy powder
CN108060322A (en) * 2017-12-07 2018-05-22 中南大学 The preparation method of hard high-entropy alloy composite material
CN109022995A (en) * 2018-07-26 2018-12-18 铜陵长江金刚石工具有限责任公司 A kind of diamond drill bit matrix and its manufacturing method
CN109136711A (en) * 2018-07-27 2019-01-04 天津立林石油机械有限公司 Novel high wear-resistant TC bearing
CN109023013A (en) * 2018-08-29 2018-12-18 中国科学院兰州化学物理研究所 A kind of preparation method of anti-corrosion and high strength AlCoCrFeNi-Cu high-entropy alloy
CN109136601A (en) * 2018-09-10 2019-01-04 南京工程学院 A kind of high hardware heart cubic phase enhances the high-entropy alloy composite material and preparation method of tough modeling face-centred cubic structure
CN109112378A (en) * 2018-09-21 2019-01-01 四川煜兴新型材料科技有限公司 A kind of preparation method of new bonding phase cemented carbide material
CN109161773A (en) * 2018-09-21 2019-01-08 成都理工大学 A kind of preparation method of high-entropy alloy bonding phase cemented carbide
CN109518057A (en) * 2018-10-11 2019-03-26 东莞理工学院 A kind of tungsten carbide material and its preparation method and application by high-entropy alloy cobalt ferronickel aluminum bronze bonding
CN109252081A (en) * 2018-10-31 2019-01-22 华南理工大学 A kind of high-entropy alloy Binder Phase ultrafine tungsten carbide hard alloy and preparation method thereof
CN109161774A (en) * 2018-11-23 2019-01-08 西安工业大学 Haystellite and preparation method thereof by high-entropy alloy as binder
CN109371307A (en) * 2018-11-29 2019-02-22 福建工程学院 It is a kind of using high-entropy alloy powder as the preparation method of the WC base cemented carbide of binder
CN110643880A (en) * 2019-11-07 2020-01-03 广东省材料与加工研究所 Drill bit matrix material and preparation method thereof
CN110684935A (en) * 2019-11-07 2020-01-14 广东省材料与加工研究所 Drill bit matrix material and preparation method thereof
CN111621661A (en) * 2020-06-09 2020-09-04 山东威尔斯通钨业有限公司 Preparation method of tungsten carbide copper
CN113073274A (en) * 2021-03-31 2021-07-06 湖南大学 Novel method for preparing double-phase ultra-fine grain high-entropy alloy

Also Published As

Publication number Publication date
CN113234982B (en) 2022-02-08

Similar Documents

Publication Publication Date Title
CN109371271B (en) Non-vacuum smelting and continuous casting process for copper-iron alloy
CN105950930B (en) A kind of solvable extruded Magnesium Alloy and preparation method thereof
CN112725649A (en) Preparation method of metal modified ceramic particle reinforced metal matrix composite material
CN110983139B (en) Magnesium alloy for staged fracturing in oil exploitation and preparation method thereof
CN103266249B (en) The drilling bit of a kind of vanadium carbide titanium Wimet and preparation thereof and preparation method
CN107119207A (en) It is a kind of non-metering than TiC enhancing Cu-base composites and preparation method thereof
CN113714488A (en) Preparation method of ceramic particle cast-in reinforced metal-based wear-resistant composite plate
CN105039836A (en) High-pressure roller mill cast-in roller surface and preparation method thereof
CN114752838A (en) Cu-Y of copper-based oxide dispersion strengthening2O3Method for preparing composite material
CN110684935B (en) Drill bit matrix material and preparation method thereof
CN113234982B (en) Preparation method of PDC drill bit matrix material
CN118291825A (en) Magnesium alloy fracturing ball for petroleum drilling and preparation method thereof
CN110983152A (en) Fe-Mn-Si-Cr-Ni based shape memory alloy and preparation method thereof
CN111041310B (en) Magnesium alloy for fracturing ball and preparation method thereof
CN113322405A (en) Hard alloy with mixed crystal structure and preparation method thereof
CN113249605B (en) Method for manufacturing metal ceramic matrix material
CN112899540A (en) Soluble magnesium alloy for oil exploitation and preparation method thereof
CN113528918A (en) Low-cobalt high-strength hard alloy and preparation method thereof
CN109913679B (en) Low-temperature matrix impregnating material of rock cutting tool and preparation method thereof
CN113699407A (en) Preparation method of graphene aluminum-based composite material
CN113528910A (en) Graphene reinforced rare earth magnesium-based composite material and preparation method thereof
CN112170862A (en) Preparation method of silver-tungsten contact material
CN100467163C (en) Method for manufacturing polycrystal diamond drill used for geological prospecting
CN116043082B (en) High-plasticity heat-resistant soluble magnesium alloy and preparation method thereof
CN111041309B (en) Soluble magnesium-based alloy and preparation method thereof

Legal Events

Date Code Title Description
PB01 Publication
PB01 Publication
SE01 Entry into force of request for substantive examination
SE01 Entry into force of request for substantive examination
GR01 Patent grant
GR01 Patent grant