CN1635174A - Preparing method for bit basis material containing rare earth - Google Patents

Preparing method for bit basis material containing rare earth Download PDF

Info

Publication number
CN1635174A
CN1635174A CN 200310116074 CN200310116074A CN1635174A CN 1635174 A CN1635174 A CN 1635174A CN 200310116074 CN200310116074 CN 200310116074 CN 200310116074 A CN200310116074 A CN 200310116074A CN 1635174 A CN1635174 A CN 1635174A
Authority
CN
China
Prior art keywords
rare earth
powder
preparation methods
bit matrix
pdc bit
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.)
Pending
Application number
CN 200310116074
Other languages
Chinese (zh)
Inventor
唐群
毛昌辉
贺从训
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.)
Beijing General Research Institute for Non Ferrous Metals
Original Assignee
Beijing General Research Institute for Non Ferrous Metals
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 Beijing General Research Institute for Non Ferrous Metals filed Critical Beijing General Research Institute for Non Ferrous Metals
Priority to CN 200310116074 priority Critical patent/CN1635174A/en
Publication of CN1635174A publication Critical patent/CN1635174A/en
Pending legal-status Critical Current

Links

Landscapes

  • Powder Metallurgy (AREA)

Abstract

The invention provides a method for preparing high strength cemented carbide basis material used for PDC drilling bit using cheap rare earth additive and common vacuum sintering technique. By adding rare-earth element in minute quantity into the raw material, and adopting common vacuum sintering technique, the shock resistance, wear resistance and fracture toughness property of the prepared PCD drilling bit basis material are all improved compared with common cemented carbide, comparing favourably with the performances of low voltage isostatic pressingsintering products but less cost of PDC drilling bit basis material.

Description

A kind of PDC bit matrix preparation methods that contains rare earth
Technical field
The present invention relates to a kind of PDC bit matrix preparation methods, particularly a kind of PDC bit matrix preparation methods that contains rare earth.
Background technology
Generally speaking, petroleum drilling is had relatively high expectations with the body material of PDC (Polycrystalline diamond composites, polycrystalline diamond matrix material) drill bit.At first require material to have higher impact-resistance; Next has certain anti-rock erosion is wear resistance; Require the material property high conformity simultaneously.
At present, quality preferably PDC bit matrix material adopt the Wimet of low pressure isostatic pressing technology sintering preparation more.This method agglomerating alloy density height, thus alloy property and life-span are increased substantially, but because the agglomerating plant costliness causes cost of alloy to increase.
Summary of the invention
The purpose of this invention is to provide a kind of cheap rare earth addition and conventional vacuum sintering technology of adopting and prepare the method for PDC drill bit with the high strength cemented carbide body material.
For achieving the above object, the present invention takes following technical scheme:
A kind of PDC bit matrix preparation methods that contains rare earth, its step is as follows:
(A) with WC powder, cobalt powder and rare earth addition mix, wherein cobalt powder accounts for 13~16 weight %, and rare earth addition accounts for 0.4~0.8 weight % of cobalt powder, and all the other are the WC powder;
(B) with above-mentioned batching through wet-milling, the precipitation, drying, the screening, mixed powder;
(C) rubber being mixed with concentration is 8~13% rubber gasoline solution;
(D) the gained rubber gasoline solution is mixed mixed powder, the add-on that makes rubber is 0.8~1.1 weight % of powder mix, and behind drying, screening, the system material, compression moulding gets pressed compact;
(E) the gained pressed compact is come unstuck under hydrogen shield;
(F) the above-mentioned pressed compact that has come unstuck is carried out vacuum sintering.
Rare earth addition is preferably yttrium oxide described in the described step (A), and other rare earth addition also can.
60~80 eye mesh screens are preferably used in screening described in the described step (B).
During vacuum sintering described in the described step (F), heat up at a slow speed during low temperature, be rapidly heated during high temperature.
During vacuum sintering described in the described step (F), under 400~450 ℃, 600~650 ℃, 800~850 ℃ and 1050~1200 ℃, be incubated 0.5 hour respectively; Finish maintenance vacuum tightness>250Pa to sintering for 1200 ℃.
Utilize the aluminium sesquioxide particle that alloy and graphite boat are separated in the vacuum sintering process described in the described step (F).
Guaranteeing on the satisfactory basis of carbon, oxygen level of raw material powder, controlling hydrogen flowing quantity well, making that graphite or scarce carbon phase appear in the unlikely alloy that causes of the variation of carbon content in the briquetting.Because cobalt contents is higher in the alloy formula,, utilize the aluminium sesquioxide particle that alloy and graphite boat are separated for preventing bottom carburizing of sintering process interalloy even sticking boat; Can reduce the volatilization of cobalt phase by the vacuum tightness of control in the sintering process, avoid that alloy is inner the carbon phase to occur lacking.
The present invention is by adding the rare earth element of trace in raw material, and the PDC bit matrix material that adopts the preparation of conventional vacuum sintering technology with shock resistance, wear resistance and fracture toughness property be improved largely than all with the ordinary rigid alloy phase, can compare favourably with low pressure isostatic sintering product properties; And compare with low pressure isostatic sintering method, because the present invention adopts the conventional vacuum sintering method, can reduce the cost of PDC bit matrix material greatly.
The present invention will be further described below by specific embodiment, but and do not mean that limiting the scope of the invention.
Embodiment
Embodiment 1
In 200 kilograms of hard gold ball grinders, add 100 kilograms of WC powder, 14 kilograms of Y that contain 0.4 weight % of cobalt powder and cobalt powder 2O 3, sintered carbide ball is 3: 1 with the compound ratio, adds 77 liters of industrial spirit, behind 24 hours batch mixings, ball milling, with 320 order phosphor-copper nets with slurry filtration, through 12~24 hours precipitations, the sucking-off supernatant liquor is being lower than under 100 ℃ the temperature the compound oven dry, and is sieving with 60~80 eye mesh screens; It is 8% rubber gasoline solution that rubber is mixed with concentration; The gained rubber gasoline solution is mixed powder mix, and the add-on that makes rubber is 0.8 weight % of powder mix, behind drying, screening, the system material, adopts compression molding method compacting standard bending strength, toughness test bar product and PDC drill bit body material; With the pressed compact processing of in 30 kilograms of hydrogen furnaces, coming unstuck, under 400~450 ℃ and 600~650 ℃, be incubated 1~2 hour respectively, then sample is carried out vacuum sintering, heat up at a slow speed when adopting low temperature (about 2~2.5 ℃/minute), the principle of (about 3~3.5 ℃/minute) is rapidly heated during high temperature, under 400~450 ℃, 600~650 ℃, 800~850 ℃ and 1050~1200 ℃, be incubated 0.5 hour respectively, finish to sintering for 1200 ℃ and keep low vacuum state (vacuum tightness>250Pa).Adopt 80~120 purpose aluminium sesquioxide particles that alloy and graphite boat are separated during sintering.
Embodiment 2
In 200 kilograms of hard gold ball grinders, add 100 kilograms of WC powder, 15 kilograms of Y that contain 0.8 weight % of cobalt powder and cobalt powder 2O 3, sintered carbide ball is 3: 1 with the compound ratio, adds 77 liters of industrial spirit, behind 24 hours batch mixings, ball milling, with 320 order phosphor-copper nets with slurry filtration, through 12~24 hours precipitations, the sucking-off supernatant liquor is being lower than under 100 ℃ the temperature the compound oven dry, and is sieving with 60~80 eye mesh screens; It is 13% rubber gasoline solution that rubber is mixed with concentration; The gained rubber gasoline solution is mixed powder mix, and the add-on that makes rubber is 1.1 weight % of powder mix, behind drying, screening, the system material, adopts compression molding method compacting standard bending strength, toughness specimen and PDC drill bit body material; With the pressed compact processing of in 30 kilograms of hydrogen furnaces, coming unstuck, under 400~450 ℃ and 600~650 ℃, be incubated 1~2 hour respectively, then sample is carried out vacuum sintering, heat up at a slow speed when adopting low temperature (about 2~2.5 ℃/minute), the principle of (about 3~3.5 ℃/minute) is rapidly heated during high temperature, under 400~450 ℃, 600~650 ℃, 800~850 ℃ and 1050~1200 ℃, be incubated 0.5 hour respectively, finish to sintering for 1200 ℃ and keep low vacuum state (vacuum tightness>250Pa).Adopt 80~120 purpose aluminium sesquioxide particles that alloy and graphite boat are separated during sintering.
Embodiment 3
In 200 kilograms of hard gold ball grinders, add 100 kilograms of WC powder, 14.5 kilograms of Y that contain 0.6 weight % of cobalt powder and cobalt powder 2O 3, sintered carbide ball is 3: 1 with the compound ratio, adds 77 liters of industrial spirit, behind 24 hours batch mixings, ball milling, with 320 order phosphor-copper nets with slurry filtration, through 12~24 hours precipitations, the sucking-off supernatant liquor is being lower than under 100 ℃ the temperature the compound oven dry, and is sieving with 60~80 eye mesh screens; It is 10% rubber gasoline solution that rubber is mixed with concentration; The gained rubber gasoline solution is mixed powder mix, and the add-on that makes rubber is 0.9 weight % of powder mix, behind drying, screening, the system material, adopts compression molding method compacting standard bending strength, toughness specimen and PDC drill bit body material; With the pressed compact processing of in 30 kilograms of hydrogen furnaces, coming unstuck, under 400~450 ℃ and 600~650 ℃, be incubated 1~2 hour respectively, then sample is carried out vacuum sintering, heat up at a slow speed when adopting low temperature (about 2~2.5 ℃/minute), the principle of (about 3~3.5 ℃/minute) is rapidly heated during high temperature, under 400~450 ℃, 600~650 ℃, 800~850 ℃ and 1050~1200 ℃, be incubated 0.5 hour respectively, finish to sintering for 1200 ℃ and keep low vacuum state (vacuum tightness>250Pa).Adopt 80~120 purpose aluminium sesquioxide particles that alloy and graphite boat are separated during sintering.
The ordinary method test shows, the common PDC bit matrix material that the bending strength of the body material of the PDC drill bit of the inventive method preparation is more congruent improves more than 20%, and impelling strength, wear resistance and fracture toughness property also are significantly improved.

Claims (7)

1, a kind of PDC bit matrix preparation methods that contains rare earth, its step is as follows:
(A) with WC powder, cobalt powder and rare earth addition mix, wherein cobalt powder accounts for 13~16 weight %, and rare earth addition accounts for 0.4~0.8 weight % of cobalt powder, and all the other are the WC powder:
(B) with above-mentioned batching through wet-milling, the precipitation, drying, the screening, mixed powder;
(C) rubber being mixed with concentration is 8~13% rubber gasoline solution;
(D) the gained rubber gasoline solution is mixed powder mix, the add-on that makes rubber is 0.8~1.1 weight % of powder mix, and behind drying, screening, the system material, compression moulding gets pressed compact;
(E) the gained pressed compact is come unstuck under hydrogen shield;
(F) the above-mentioned pressed compact that has come unstuck is carried out vacuum sintering.
2, the PDC bit matrix preparation methods that contains rare earth according to claim 1, it is characterized in that: rare earth addition is a yttrium oxide described in the described step (A).
3, the PDC bit matrix preparation methods that contains rare earth according to claim 1 and 2 is characterized in that: 60~80 eye mesh screens are used in screening described in the described step (B).
4, the PDC bit matrix preparation methods that contains rare earth according to claim 3 is characterized in that: during vacuum sintering described in the described step (F), heat up at a slow speed during low temperature, be rapidly heated during high temperature.
5, the PDC bit matrix preparation methods that contains rare earth according to claim 4, it is characterized in that: it is 2~2.5 ℃/minute that described low temperature heats up at a slow speed; It is 3~3.5 ℃/minute that described high temperature is rapidly heated.
6, the PDC bit matrix preparation methods that contains rare earth according to claim 4, it is characterized in that: during vacuum sintering described in the described step (F), under 400~450 ℃, 600~650 ℃, 800~850 ℃ and 1050~1200 ℃, be incubated 0.5 hour respectively; Finish maintenance vacuum tightness>250Pa to sintering for 1200 ℃.
7, according to claim 5 or the 6 described PDC bit matrix preparation methods that contain rare earth, it is characterized in that: utilize the aluminium sesquioxide particle that alloy and graphite boat are separated in the vacuum sintering process described in the described step (F).
CN 200310116074 2003-12-30 2003-12-30 Preparing method for bit basis material containing rare earth Pending CN1635174A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN 200310116074 CN1635174A (en) 2003-12-30 2003-12-30 Preparing method for bit basis material containing rare earth

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN 200310116074 CN1635174A (en) 2003-12-30 2003-12-30 Preparing method for bit basis material containing rare earth

Publications (1)

Publication Number Publication Date
CN1635174A true CN1635174A (en) 2005-07-06

Family

ID=34843554

Family Applications (1)

Application Number Title Priority Date Filing Date
CN 200310116074 Pending CN1635174A (en) 2003-12-30 2003-12-30 Preparing method for bit basis material containing rare earth

Country Status (1)

Country Link
CN (1) CN1635174A (en)

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN100462463C (en) * 2006-03-30 2009-02-18 中南大学 Material for eliminating impurity inside metallurgical furnace
CN101016826B (en) * 2007-03-08 2010-06-16 江汉石油钻头股份有限公司 Bit body of diamond bit and manufacture method therefor
CN101704101B (en) * 2009-11-27 2012-03-28 西南石油大学 Formula and technique for manufacturing geophysical prospecting bit by powder sintering
CN104439248A (en) * 2014-12-05 2015-03-25 江西耀升钨业股份有限公司 Preparation method of diamond enhanced tungsten carbide composite spherical crown button with gradient structure
CN105618736A (en) * 2016-02-21 2016-06-01 刘辉 Reamer bit
CN108380818A (en) * 2018-04-12 2018-08-10 北京科技大学 The method that isostatic cool pressing combination lost foam prepares Metal Substrate SHS wear-resistant coatings
CN109518058A (en) * 2018-12-06 2019-03-26 宇龙精机科技(浙江)有限公司 A kind of deep-hole drill bit hard alloy and preparation method thereof

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN100462463C (en) * 2006-03-30 2009-02-18 中南大学 Material for eliminating impurity inside metallurgical furnace
CN101016826B (en) * 2007-03-08 2010-06-16 江汉石油钻头股份有限公司 Bit body of diamond bit and manufacture method therefor
CN101704101B (en) * 2009-11-27 2012-03-28 西南石油大学 Formula and technique for manufacturing geophysical prospecting bit by powder sintering
CN104439248A (en) * 2014-12-05 2015-03-25 江西耀升钨业股份有限公司 Preparation method of diamond enhanced tungsten carbide composite spherical crown button with gradient structure
CN105618736A (en) * 2016-02-21 2016-06-01 刘辉 Reamer bit
CN108380818A (en) * 2018-04-12 2018-08-10 北京科技大学 The method that isostatic cool pressing combination lost foam prepares Metal Substrate SHS wear-resistant coatings
CN109518058A (en) * 2018-12-06 2019-03-26 宇龙精机科技(浙江)有限公司 A kind of deep-hole drill bit hard alloy and preparation method thereof

Similar Documents

Publication Publication Date Title
CN101985717B (en) Method for preparing high-tenacity super-coarse-grained tungsten and cobalt hard alloy
CN101121983B (en) Method for preparing coarse grain hard alloy and the coarse grain hard alloy
CN102990069B (en) A kind of preparation method utilizing useless tungsten-cobalt alloy to make coarse-grain carbide alloy pick
CN107758666B (en) (Ti, M) C nano solid solution powder and preparation method thereof
CN102534277B (en) New preparation method for coarse particles and super coarse particle hard alloy
CN109576545B (en) Ti (C, N) -based metal ceramic with mixed crystal structure and preparation method thereof
CN1118812A (en) Tungsten-based cemented carbide powder mix and cemented carbide products made therefrom
CN1837040A (en) Process for self-propagating high-temperature synthesis of nano tungsten carbide powder
CN1635174A (en) Preparing method for bit basis material containing rare earth
CN106756391A (en) A kind of WC Co hard alloy preparation methods with duplex grain structure
CN103911536A (en) Cr containing high-grade steel hard alloy cutter material for petroleum pipeline thread machining
CN100458241C (en) Light hard alloy seal ring and producing method thereof
CN105296834B (en) High-hardness and high-tenacity hard alloy and preparation method thereof
CN107245626B (en) A kind of method of high entropy effect enhancing (W, Ti, V) C-Co hard alloy mechanical property
CN114262833B (en) High-entropy carbide-reinforced TiCN-based metal ceramic with high hardness and high toughness and preparation method and application thereof
CN111455250A (en) Hard alloy material for crushing iron ore and preparation method thereof
CN1654425A (en) Method for in-situ hot-pressing synthesis of compact Ti3SiC2-Al2O3 composite blocks
CN109518057A (en) A kind of tungsten carbide material and its preparation method and application by high-entropy alloy cobalt ferronickel aluminum bronze bonding
CN85100348A (en) Twin crystal optimization is than the method for making that is 2.2 tungsten-cobalt carbide alloy
CN112609116B (en) Hard alloy for strengthening Co-Ni-based binder phase through Si and preparation method thereof
CN110846546B (en) Method for preparing high-strength and high-toughness hard alloy by using pre-alloy powder
CN112430460B (en) Petroleum fracturing propping agent and preparation method and application thereof
CN1542148A (en) Method for producing metallic chromium
CN101033135A (en) Aluminum oxide enhanced titanium-silicon-aluminum-carbon base ceramics composite material and preparing method thereof
CN1569732A (en) Rare earth reinforced alumina ceramic composite materials and production method thereof

Legal Events

Date Code Title Description
C06 Publication
PB01 Publication
C10 Entry into substantive examination
SE01 Entry into force of request for substantive examination
C02 Deemed withdrawal of patent application after publication (patent law 2001)
WD01 Invention patent application deemed withdrawn after publication