CN106756168A - The method that one kind prepares Ti (C, N) based ceramic metal based on carbon thermal reduction molybdenum trioxide - Google Patents

The method that one kind prepares Ti (C, N) based ceramic metal based on carbon thermal reduction molybdenum trioxide Download PDF

Info

Publication number
CN106756168A
CN106756168A CN201611135714.9A CN201611135714A CN106756168A CN 106756168 A CN106756168 A CN 106756168A CN 201611135714 A CN201611135714 A CN 201611135714A CN 106756168 A CN106756168 A CN 106756168A
Authority
CN
China
Prior art keywords
ceramic metal
molybdenum trioxide
based ceramic
vacuum
forming agent
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
CN201611135714.9A
Other languages
Chinese (zh)
Other versions
CN106756168B (en
Inventor
郑勇
周伟
赵毅杰
张家杰
章国涛
柯峥
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.)
Nanjing University of Aeronautics and Astronautics
Original Assignee
Nanjing University of Aeronautics and Astronautics
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 Nanjing University of Aeronautics and Astronautics filed Critical Nanjing University of Aeronautics and Astronautics
Priority to CN201611135714.9A priority Critical patent/CN106756168B/en
Publication of CN106756168A publication Critical patent/CN106756168A/en
Application granted granted Critical
Publication of CN106756168B publication Critical patent/CN106756168B/en
Active legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22CALLOYS
    • C22C1/00Making non-ferrous alloys
    • C22C1/04Making non-ferrous alloys by powder metallurgy
    • C22C1/05Mixtures of metal powder with non-metallic powder
    • C22C1/051Making hard metals based on borides, carbides, nitrides, oxides or silicides; Preparation of the powder mixture used as the starting material therefor
    • C22C1/053Making hard metals based on borides, carbides, nitrides, oxides or silicides; Preparation of the powder mixture used as the starting material therefor with in situ formation of hard compounds
    • C22C1/055Making hard metals based on borides, carbides, nitrides, oxides or silicides; Preparation of the powder mixture used as the starting material therefor with in situ formation of hard compounds using carbon
    • 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
    • C22C29/005Alloys based on carbides, oxides, nitrides, borides, or silicides, e.g. cermets, or other metal compounds, e.g. oxynitrides, sulfides comprising a particular metallic binder
    • 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
    • C22C29/04Alloys 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 carbonitrides

Landscapes

  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Mechanical Engineering (AREA)
  • Metallurgy (AREA)
  • Organic Chemistry (AREA)
  • Powder Metallurgy (AREA)
  • Ceramic Products (AREA)

Abstract

The invention discloses the method that one kind prepares Ti (C, N) based ceramic metal based on carbon thermal reduction molybdenum trioxide, the cermet composition mass fraction is as follows:Ti is that 31.5~39.7, C is that 10.6~11, N is that 3.6~4.6, O is that 5.4~6.6, Ni is that 22~31, Mo is that 10~12.4, W is 4.2~7.7.Preparation method feature is:When compound is prepared, with molybdenum trioxide as molybdenum source, it is directly appended in compound, then in turn through batch mixing, adds forming agent, compressing, removing forming agent and use special combination vacuum sintering method, is obtained the sintered cermet of densification.The present invention can be greatly reduced production cost, and be effectively improved the microscopic structure of cermet, improve its mechanical property, have broad application prospects.

Description

The method that one kind prepares Ti (C, N) based ceramic metal based on carbon thermal reduction molybdenum trioxide
Technical field
The present invention relates to the method that one kind prepares Ti (C, N) based ceramic metal based on carbon thermal reduction molybdenum trioxide, belong to powder Last metallurgical technology field.
Background technology
Ti (C, N) based ceramic metal has that density is low, red hardness is high, wearability is high, high temperature and creep resistance ability and anti-oxidant Ability is strong and the advantages of intermetallic coefficient of friction is low, corrosion resistance is good, in cutter, mould, wear-resisting spare part, corrosion-resistant device Gathered around etc. various fields and had broad application prospects.Such as it is used as cutter material, compared with conventional hard alloy cutter, it can permit Permitted to have cutting speed higher and the larger depth of cut, anti-crescent hollow abrasion ability be higher, workpiece to be machined surface quality is more preferable; Such as it is used as mold materials, not only red hardness is high, heat endurance and oxidation resistant, and good toughness;Such as it is used as wear-resisting and corrosion resistant Corrosion material, its service life is higher compared to similar other materials.In recent years, hair of Ti (C, the N) based ceramic metals in countries in the world Exhibition is all very rapid.
The subject matter that Ti (C, N) based ceramic metal of exploitation is present at present is under conditions of certain degree of hardness is kept, to resist Curved intensity and fracture toughness are still relatively low, make its in theory due advantage be not not fully exerted, so as to cause it to apply Scope is subject to certain restrictions.In the last few years, some researchers by attempt introducing all kinds of whiskers, CNT wait until Ti (C, N) in based ceramic metal, the activeness and quietness of cermet is realized.The above method makes although obtaining relatively good experimental result The obdurability of Ti (C, N) based ceramic metal has a certain degree of raising.But, the additive such as whisker, CNT price is held high It is expensive, and purity also needs further raising, is easy to oxygen uptake and reunion.Before being added in compound, it is necessary to carry out removal of impurities, take off The pre-treatment such as oxygen and dispersion.Above-mentioned additive is not only very expensive, and is difficult to be evenly distributed in compound, makes cermet Preparation cost significantly rise, preparation technology complexity substantially increases, and in batch production, it is easy to form metallurgical lacking Fall into, substandard products occur, thus be difficult in industrial circle obtain practical application so far.On the other hand, researcher also is burnt using hot pressing The special sintering method such as knot, low pressure-HIP sintering, discharge plasma sintering prepares Ti (C, N) Base Metal pottery of fine grain Porcelain, makes the performance of material obtain a certain degree of raising, but these special sintering methods are higher to equipment requirement, early investment It is larger, and production cost significantly improves.
In view of the foregoing, in order that Ti (C, N) based ceramic metal can be applied in more areas, it is necessary to this kind of Material is further studied, and develops a kind of Ti of high-performance and low-cost (C, N) based ceramic metal.
The content of the invention
For above-mentioned technical problem, Ti is prepared based on carbon thermal reduction molybdenum trioxide it is an object of the invention to provide one kind The method of (C, N) based ceramic metal.The method can prepare that comprehensive mechanical property is higher, stable performance Ti (C, N) fund Category ceramics, and it is cheap for manufacturing cost.
Realizing the technical solution of the object of the invention is:
The method that one kind prepares Ti (C, N) based ceramic metal based on carbon thermal reduction molybdenum trioxide, comprises the following steps that:
1) component of preparation compound, including following mass fraction:Ti is 31.5~39.7, C for 10.6~11, N is 3.6 ~4.6, O are that 5.4~6.6, Ni is that 22~31, Mo is that 10~12.4, W is 4.2~7.7;
When preparing the compound of mentioned component, raw materials used is Ti (C, N) solid solution powder, MoO3Powder, WC powder, Ni powder, powder The granularity at end is micron order;
2) batch mixing is carried out in planetary ball mill, drum's speed of rotation is 300~400rpm, and the time is 24~36h;
3) add forming agent, shaping agent concentration be 7wt.% polyvinyl alcohol water solutions, additional proportion be compound 3~ 5wt%;
4) it is compressing under 150~200MPa of pressing pressure;
5) forming agent is removed in vacuum drying oven of the vacuum higher than 10Pa, the programming rate between 200~400 DEG C is 0.3~0.4 DEG C/min;
6) vacuum-sintering, is carried out in vacuum sintering furnace, and vacuum is higher than 1.0 × 10-2Pa;Described vacuum-sintering is divided into Four-stage, is continuously heating to 600~800 DEG C by the pressed compact for removing forming agent first, is incubated 2~4h;Then raise temperature to 1200 ~1240 DEG C, it is incubated 1~2h;Then 1400~1440 DEG C are warming up to again, are incubated 0.5~1h;The last cooling with 20 DEG C/min Speed makes furnace temperature quickly be down to less than 1000 DEG C, obtains Ti (C, N) based ceramic metal.
To realize this purpose, step 1 of the present invention) in prepare compound when, the Mo in compound is with MoO3The form of powder is drawn Enter.In general, in Ti (C, N) based ceramic metal, oxygen is considered as harmful element, because their meetings in liquid sintering process The angle of wetting between hard phase and Binder Phase is become big, reduce its wetability, so that deteriorate materials microstructure and performance, so mesh The preceding oxygen content in all powder is reduced as far as possible during preparing cermet.The present invention is with MoO3The form of powder is by Mo It is incorporated into Ti (C, N) based ceramic metal compound with O elements, while introducing the C of corresponding content in the form of graphite powder, is led to Cross rationally control sintering process, MoO3There is following solid phase reaction before 800 DEG C with graphite powder in powder:MoO3+C→MoO2+CO; MoO2+2C→Mo+2CO;2Mo+C→Mo2C, it is in situ that O is removed and Mo is generated with C chemical combination2C.And now sintered body is still in preceding The solid-phase sintering stage of phase, its relative density is relatively low, and hole is in perforate state, and the gas for reacting generation under vacuum can Smoothly effusion, will not have a negative impact to follow-up liquid-phase sintering.Meanwhile, introduced a large amount of graphite powders and MoO3Powder occurs The reducibility gas CO discharged in carbothermic reduction process can make more thorough, the purification of the absorption oxygen removal on other original powder surfaces Interface between ceramic phase and metallic binding phase, is effectively improved the microscopic structure of cermet, strengthens the bond strength of boundary, The purpose of Ti (C, N) based ceramic metal obdurability is improved so as to reach.
To realize this purpose, preparation method has following features:Vacuum-sintering is divided into four-stage, is first molded removing The pressed compact of agent is warming up to 600~800 DEG C, is incubated 2~4h;1200~1240 DEG C are then raised temperature to, 1~2h is incubated;Then rise again Temperature is incubated 0.5~1h to 1400~1440 DEG C;The last cooling velocity with 20 DEG C/min make furnace temperature be quickly down to 1000 DEG C with Under.It is to allow MoO that 2~4h is incubated at 600~800 DEG C3Powder and graphite powder pass through carbothermic reduction reaction in situ and generate Mo2C;With After be warming up to 1200~1240 DEG C, 1~2h of insulation is in order that the Mo of generation2WC and Ti (C, N) solid solution in C, compound Annular phase is formed in ceramic hard phase particle surface by solid phase reaction, to improve following liquid-phase sintering stage metal adhesive phase To the wetability of ceramic phase, and prevent crystal grain agglomeration;1400~1440 DEG C are warming up to, 0.5~1h of insulation is in order that gold Category ceramics enter the liquid-phase sintering stage, complete densification and the microstructure homogenization of sintered body;The last cooling speed with 20 DEG C/min Degree makes furnace temperature quickly be down to less than 1000 DEG C, is in order that sintered body rapid solidification, prevents ceramic hard from stopping in liquid phase stage Overlong time is stayed too to be grown up by crystallization of the dissolution and precipitation mechanism.
Beneficial effect of the present invention is:
1st, Ti (C, N) based ceramic metal prepared based on carbon thermal reduction molybdenum trioxide that the present invention is provided, with higher Comprehensive mechanical property, and its hardness, bending strength and fracture toughness can adjust according to the performance requirement in different application field.Institute The cermet material of preparation is not only with red hardness is good, wearability is high, oxidation resistance is strong and intermetallic coefficient of friction is low The advantages of, and obdurability and stability significantly improve, and cannot be only used for Tool in Cutting field, be equally applicable to mine, The fields such as oil, coal mining, can also be widely used as wearing piece, high temperature resistant part, corrosion barrier etc..
What the 2nd, the present invention was provided is free of valuable unit based on Ti (C, N) based ceramic metal prepared by carbon thermal reduction molybdenum trioxide Element, the MoO as Mo sources3Powder price is with respect to Mo powder or Mo2C powder is cheaper, and cost of material is cheaper.
What the 3rd, the present invention was provided uses the true of routine based on Ti (C, N) based ceramic metal prepared by carbon thermal reduction molybdenum trioxide Prepared by empty sintering process, to production equipment without particular/special requirement, be conducive to commercial introduction application;Technical process is simple, complete at one Thermal cycle in complete, can significantly saving energy consumption, reduce production cost, improve productivity ratio.
Specific embodiment
Technique effect of the invention is further illustrated below in conjunction with example.The raw material that following instance is used is Ti (C, N) Powder, Ni powder, MoO3Powder, WC powder, graphite powder.
Table 1 is 4 kinds of compounds of component prescription.It is prepared by three kinds of different technical parameters that embodiment 1-3 is respectively adopted Into Ti (C, N) based ceramic metal, and its hardness, bending strength and palmqvist fracture toughnesses are determined respectively, wherein 1#With 2#Into Metallic binding phase is relatively low in distribution side, and hardness is higher, it is adaptable to cutting tool and wearing piece field, 3#With 4#Gold in component prescription Category Binder Phase is higher, and obdurability is preferable, it is adaptable to the part needed for making the fields such as mine, oil, coal mining.
1 four kinds of component prescriptions of compound of table
Composition Ti C N O Ni Mo W
1# 39.7 10.6 4.6 5.4 22 10 7.7
2# 37.2 11 4.3 5.8 25 10.8 5.9
3# 33.2 10.8 3.9 6.4 28 11.6 6.1
4# 31.5 10.7 3.6 6.6 31 12.4 4.2
Embodiment 1:
1st, 4 kinds of compounds are prepared according to table 1;
2nd, compound is placed in planetary ball mill and is mixed, drum's speed of rotation is 300rpm, the time is 36h;
3rd, forming agent is added:It is the polyvinyl alcohol water solution of 7wt.% that forming agent uses concentration, and addition is compound 3wt%;
4th, it is compressing:Compressing pressure used is 150MPa;
5th, forming agent is removed:Removing forming agent operation is carried out in vacuum sintering furnace, and vacuum is higher than 10Pa, 200~ Programming rate between 400 DEG C is 0.3 DEG C/min;
6th, vacuum-sintering:Carried out in vacuum sintering furnace, vacuum is higher than 1.0 × 10-2Pa.Vacuum-sintering is divided into four ranks Section, is continuously heating to 600 DEG C by the pressed compact for removing forming agent first, is incubated 4h;1240 DEG C are then raised temperature to, 1h is incubated;Then 1440 DEG C are warming up to again, are incubated 30min;The last cooling velocity with 20 DEG C/min makes furnace temperature quickly be down to less than 1000 DEG C, obtains To Ti (C, N) based ceramic metal.
Under above-mentioned preparation process condition, the mechanical property of the cermet of heterogeneity formula is shown in Table 2.
The mechanical property of the different metal ceramics that table 2 is prepared using technique 1
Composition 1# 2# 3# 4#
Bending strength σb(MPa) 1715 1938 2217 2461
Hardness (HRA) 92.3 91.1 89.7 88.0
Fracture toughness (MNm-3/2) 12.4 14.6 17.9 22.3
Embodiment 2:
1st, 4 kinds of compounds are prepared according to table 1;
2nd, compound is placed in planetary ball mill and is mixed, drum's speed of rotation is 350rpm, the time is 30h;
3rd, forming agent is added:It is the polyvinyl alcohol water solution of 7wt.% that forming agent uses concentration, and addition is compound 4wt%;
4th, it is compressing:Compressing pressure used is 180MPa;
5th, forming agent is removed:Removing forming agent operation is carried out in vacuum sintering furnace, and vacuum is higher than 10Pa, 200~ Programming rate between 400 DEG C is 0.4 DEG C/min;
6th, vacuum-sintering:Carried out in vacuum sintering furnace, vacuum is higher than 1.0 × 10-2Pa.Vacuum-sintering is divided into four ranks Section, is continuously heating to 700 DEG C by the pressed compact for removing forming agent first, is incubated 3h;1220 DEG C are then raised temperature to, 1.5h is incubated;So It is warming up to 1420 DEG C again afterwards, is incubated 40min;The last cooling velocity with 20 DEG C/min makes furnace temperature quickly be down to less than 1000 DEG C, Obtain Ti (C, N) based ceramic metal.
Under above-mentioned preparation process condition, the performance of the cermet of heterogeneity proportioning is shown in Table 3.
The mechanical property of the different metal ceramics that table 3 is prepared using technique 2
Composition 1# 2# 3# 4#
Bending strength σb(MPa) 1724 2017 2256 2473
Hardness (HRA) 92.1 91.0 89.5 88.2
Fracture toughness (MNm-3/2) 11.8 14.3 18.1 22.5
Embodiment 3:
1st, 4 kinds of compounds are prepared according to table 1;
2nd, compound is placed in planetary ball mill and is mixed, drum's speed of rotation is 400rpm, the time is 24h;
3rd, forming agent is added:It is the polyvinyl alcohol water solution of 7wt.% that forming agent uses concentration, and addition is compound 5wt%;
4th, it is compressing:Compressing pressure used is 200MPa;
5th, forming agent is removed:Removing forming agent operation is carried out in vacuum sintering furnace, and vacuum is higher than 10Pa, 200~ Programming rate between 400 DEG C is 0.4 DEG C/min;
6th, vacuum-sintering:Carried out in vacuum sintering furnace, vacuum is higher than 1.0 × 10-2Pa.Vacuum-sintering is divided into four ranks Section, is continuously heating to 800 DEG C by the pressed compact for removing forming agent first, is incubated 2h;1200 DEG C are then raised temperature to, 2h is incubated;Then 1400 DEG C are warming up to again, are incubated 1h;The last cooling velocity with 20 DEG C/min makes furnace temperature quickly be down to less than 1000 DEG C, obtains Ti (C, N) based ceramic metal.
Under above-mentioned preparation process condition, the performance of the cermet of heterogeneity proportioning is shown in Table 4.
The mechanical property of the different metal ceramics that table 4 is prepared using technique 3
Composition 1# 2# 3# 4#
Bending strength σb(MPa) 1709 1997 2233 2469
Hardness (HRA) 92.0 91.2 89.4 88.1
Fracture toughness (MNm-3/2) 12.1 14.1 18.3 21.9
In this letter of authorization span, the technological parameter of sintering process first stage is relatively large to performance impact, only Have when this stage sintering temperature and soaking time collocation it is reasonable when (when holding temperature is higher, the time accordingly shortens;Holding temperature When relatively low, the time answers proper extension), the cermet of above-mentioned each component prescription can obtain relatively good comprehensive mechanical property. In a word, in claims span, its influence to material mechanical performance of above-mentioned technological factor is limited.
The above embodiments are intended to illustrate the present invention, rather than limitation, therefore with it is of the invention Any change in claims suitable implication and scope, is all considered as being included within the scope of the claims.
Concrete application approach of the present invention is a lot, and the above is only the preferred embodiment of the present invention, it is noted that for For those skilled in the art, under the premise without departing from the principles of the invention, some improvement can also be made, such as Other constituent elements are substituted with corresponding oxide, and oxide are reduced by carbothermic method in situ in sintering process, These improvement also should be regarded as protection scope of the present invention.

Claims (6)

1. it is a kind of to be based on the method that carbon thermal reduction molybdenum trioxide prepares Ti (C, N) based ceramic metal, it is characterised in that including following Step:
1) component of preparation compound, including following mass fraction:Ti be 31.5~39.7, C be 10.6~11, N be 3.6~ 4.6, O is that 5.4~6.6, Ni is that 22~31, Mo is that 10~12.4, W is 4.2~7.7;
2) batch mixing;
3) forming agent is added;
4) it is compressing;
5) forming agent is removed;
6) vacuum-sintering, is carried out in vacuum sintering furnace, and vacuum is higher than 1.0 × 10-2Pa;Described vacuum-sintering is divided into four In the stage, the pressed compact removed after forming agent is continuously heating to 600~800 DEG C first, is incubated 2~4h;Then raise temperature to 1200~ 1240 DEG C, it is incubated 1~2h;Then 1400~1440 DEG C are warming up to again, are incubated 0.5~1h;The last cooling speed with 20 DEG C/min Degree makes furnace temperature quickly be down to less than 1000 DEG C, obtains Ti (C, N) based ceramic metal.
2. the method that Ti (C, N) based ceramic metal is prepared based on carbon thermal reduction molybdenum trioxide according to claim 1, it is special Levy and be:When preparing the compound of mentioned component, raw materials used is Ti (C, N) solid solution powder, MoO3Powder, WC powder, Ni powder, powder Granularity be micron order.
3. the method that Ti (C, N) based ceramic metal is prepared based on carbon thermal reduction molybdenum trioxide according to claim 1, it is special Levy and be:The step 2) in compounding process carried out in planetary ball mill, drum's speed of rotation be 300~400rpm, when Between be 24~36h.
4. the method that Ti (C, N) based ceramic metal is prepared based on carbon thermal reduction molybdenum trioxide according to claim 1, it is special Levy and be:Described step 3) in forming agent used be concentration be 7wt.% polyvinyl alcohol water solutions, additional proportion is compound 3~5wt%.
5. the method that Ti (C, N) based ceramic metal is prepared based on carbon thermal reduction molybdenum trioxide according to claim 1, it is special Levy and be:Described step 4) in pressing pressure used by compressing operation be 150~200MPa.
6. the method that Ti (C, N) based ceramic metal is prepared based on carbon thermal reduction molybdenum trioxide according to claim 1, it is special Levy and be:Described step 5) in removing forming agent operation carried out in vacuum drying oven of the vacuum higher than 10Pa, 200~ Programming rate between 400 DEG C is 0.3~0.4 DEG C/min.
CN201611135714.9A 2016-12-12 2016-12-12 The method that one kind prepares Ti (C, N) based ceramic metal based on carbon thermal reduction molybdenum trioxide Active CN106756168B (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN201611135714.9A CN106756168B (en) 2016-12-12 2016-12-12 The method that one kind prepares Ti (C, N) based ceramic metal based on carbon thermal reduction molybdenum trioxide

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN201611135714.9A CN106756168B (en) 2016-12-12 2016-12-12 The method that one kind prepares Ti (C, N) based ceramic metal based on carbon thermal reduction molybdenum trioxide

Publications (2)

Publication Number Publication Date
CN106756168A true CN106756168A (en) 2017-05-31
CN106756168B CN106756168B (en) 2018-05-22

Family

ID=58879813

Family Applications (1)

Application Number Title Priority Date Filing Date
CN201611135714.9A Active CN106756168B (en) 2016-12-12 2016-12-12 The method that one kind prepares Ti (C, N) based ceramic metal based on carbon thermal reduction molybdenum trioxide

Country Status (1)

Country Link
CN (1) CN106756168B (en)

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN109487141A (en) * 2018-12-12 2019-03-19 南京航空航天大学 A kind of preparation method of plate carbide solid solution toughening mixed crystal Ti (C, N) based ceramic metal
CN109576545A (en) * 2018-12-12 2019-04-05 南京航空航天大学 A kind of Ti (C, N) based ceramic metal and preparation method thereof with duplex grain structure
CN110408830A (en) * 2019-08-28 2019-11-05 三峡大学 A kind of Ti (C, N) base metal-ceramic material and its Carbon balance control method
CN114752835A (en) * 2022-03-18 2022-07-15 南京航空航天大学 Ti (C, N) -based metal ceramic with honeycomb structure and preparation method thereof

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5756410A (en) * 1997-02-27 1998-05-26 The Dow Chemical Company Method for making submicrometer transition metal carbonitrides
CN1410575A (en) * 2002-12-02 2003-04-16 株洲硬质合金集团有限公司 Metal ceramic and its preparation method
CN104131192A (en) * 2014-07-25 2014-11-05 常熟市鼎丰金属材料科技有限公司 Ti(C,N)-based metal ceramic with gradient structure and plasma-nitriding preparation method thereof

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5756410A (en) * 1997-02-27 1998-05-26 The Dow Chemical Company Method for making submicrometer transition metal carbonitrides
CN1410575A (en) * 2002-12-02 2003-04-16 株洲硬质合金集团有限公司 Metal ceramic and its preparation method
CN104131192A (en) * 2014-07-25 2014-11-05 常熟市鼎丰金属材料科技有限公司 Ti(C,N)-based metal ceramic with gradient structure and plasma-nitriding preparation method thereof

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
ASAO OYA ET AL.: "Carbothermal Reduction of the Molybdenum Oxide/Phenanthroline Complex", 《JOURNAL OF THE AMERICAN CERAMIC SOCIETY》 *

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN109487141A (en) * 2018-12-12 2019-03-19 南京航空航天大学 A kind of preparation method of plate carbide solid solution toughening mixed crystal Ti (C, N) based ceramic metal
CN109576545A (en) * 2018-12-12 2019-04-05 南京航空航天大学 A kind of Ti (C, N) based ceramic metal and preparation method thereof with duplex grain structure
CN109576545B (en) * 2018-12-12 2020-09-25 南京航空航天大学 Ti (C, N) -based metal ceramic with mixed crystal structure and preparation method thereof
CN110408830A (en) * 2019-08-28 2019-11-05 三峡大学 A kind of Ti (C, N) base metal-ceramic material and its Carbon balance control method
CN114752835A (en) * 2022-03-18 2022-07-15 南京航空航天大学 Ti (C, N) -based metal ceramic with honeycomb structure and preparation method thereof
CN114752835B (en) * 2022-03-18 2022-10-25 南京航空航天大学 Ti (C, N) -based metal ceramic with honeycomb structure and preparation method thereof

Also Published As

Publication number Publication date
CN106756168B (en) 2018-05-22

Similar Documents

Publication Publication Date Title
CN107475548B (en) A kind of preparation method of nanometer of toughening superfine WC-Co cemented carbide
CN102717086B (en) Method for preparing high-niobium titanium-aluminum alloy spherical micro powder in short process
CN100567530C (en) A kind of preparation method of high performance sinter Mo-Ti-Zr molybdenum alloy
CN106756168B (en) The method that one kind prepares Ti (C, N) based ceramic metal based on carbon thermal reduction molybdenum trioxide
CN104313380B (en) A kind of step sintering prepares the method for high-compactness Nanograin Cemented Carbide
CN103572087B (en) The preparation method of boron carbide particles reinforced aluminum matrix composites
CN109338172A (en) A kind of 2024 aluminum matrix composites and preparation method thereof of high-entropy alloy enhancing
CN107663607A (en) A kind of high-entropy alloy holds composite of abrasive grain and its preparation method and application
CN110102752B (en) Solid solution alloy powder for metal ceramic and preparation method thereof
CN107096924A (en) The preparation method and product of a kind of spherical metal base rare earth nano composite powder available for 3 D-printing
CN111069614B (en) Additive manufacturing method of in-situ synthesized micro-nano TiC reinforced titanium-based composite material
CN109338193B (en) Coreless-ring structure metal ceramic alloy and preparation method thereof
CN109487141A (en) A kind of preparation method of plate carbide solid solution toughening mixed crystal Ti (C, N) based ceramic metal
CN109576545A (en) A kind of Ti (C, N) based ceramic metal and preparation method thereof with duplex grain structure
CN106756391A (en) A kind of WC Co hard alloy preparation methods with duplex grain structure
CN107971499A (en) The method for preparing spherical titanium aluminium-based alloyed powder end
CN103240421B (en) A kind of production method of high-pressure blank intensity tungsten powder and system
CN109014230A (en) A kind of preparation method of molybdenum grid
CN109332717B (en) Preparation method of spherical molybdenum titanium zirconium alloy powder
CN102127714A (en) Nano-cluster-strengthened iron-base superalloy
CN107641725A (en) A kind of ferrosilite based ceramic metal and preparation method thereof
CN109778046B (en) Preparation method of low-cost high-performance WC-Co hard alloy with mixed crystal structure
CN110983152A (en) Fe-Mn-Si-Cr-Ni based shape memory alloy and preparation method thereof
CN102091859B (en) High-density tungsten alloy complex part molding process
CN105710380A (en) Aluminum-contained metal printing powder 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