CN101811190B - In-situ TiB2 and Ti5Si3 composite material and preparation method thereof - Google Patents

In-situ TiB2 and Ti5Si3 composite material and preparation method thereof Download PDF

Info

Publication number
CN101811190B
CN101811190B CN2010191000120A CN201019100012A CN101811190B CN 101811190 B CN101811190 B CN 101811190B CN 2010191000120 A CN2010191000120 A CN 2010191000120A CN 201019100012 A CN201019100012 A CN 201019100012A CN 101811190 B CN101811190 B CN 101811190B
Authority
CN
China
Prior art keywords
powder
tib
reactant
pressed compact
original position
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.)
Active
Application number
CN2010191000120A
Other languages
Chinese (zh)
Other versions
CN101811190A (en
Inventor
王慧远
姜启川
吕思婕
李进彪
杨治政
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.)
Jilin University
Original Assignee
Jilin 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 Jilin University filed Critical Jilin University
Priority to CN2010191000120A priority Critical patent/CN101811190B/en
Publication of CN101811190A publication Critical patent/CN101811190A/en
Application granted granted Critical
Publication of CN101811190B publication Critical patent/CN101811190B/en
Active legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Abstract

The invention relates to an in-situ TiB2 and Ti5Si3 composite material and a preparation method thereof. The composite material comprises in-situ TiB2 and Ti5Si3, wherein the in-situ TiB2 is 1 to 20 percent based on the mass of TiB2. The preparation method comprises the following steps: 1) mixing B powder, Si powder and Ti powder, which serve as reactants, uniformly according to a certain proportion and pressing the reactants into billets; 2) preheating the reactant billets in an argon atmosphere and then heating the reactant billets again until a combustion synthesis reaction occurs, or igniting the bottom end of the reactant billets by using arc heat generated by a tungsten electrode to initiate the combustion synthesis reaction; and 3) after the reaction, pressurizing and compacting the reaction product to form the TiB2 and Ti5Si3 composite material. The material has the advantages of excellent performance such as high strength and high hardness, obvious reinforcement effect due to metallurgical combination between reinforcements and a matrix, convenient preparation process, simple equipment, low energy consumption and easy popularization and application.

Description

A kind of original position TiB<sub〉2</sub 〉-Ti<sub〉5</sub〉Si<sub〉3</sub〉composite and preparation method thereof
Technical field
The present invention relates to field of compound material, particularly relate to a kind of original position TiB 2-Ti 5Si 3Composite and preparation method thereof.
Background technology
Because compound Ti between refractory metal 5Si 3Have good high-temperature intensity and creep-resistant property, and excellent high-temperature oxidation resistance and decay resistance and enjoy favor.But, Ti 5Si 3Room temperature fragility big, fracture toughness is low, has limited its application.From the inherent attribute of material, compoundization is to solve Ti 5Si 3The effective way of fragility problem.In recent years, more about the research of compound composite material between bimetallic in the world, and adopt the research of Ceramic Composite intermetallic compound less relatively.The research paper that is published in " Materials Science and Engineering A, 1999,269:129-135 " shows that percent by volume is 20 ZrO 2And Ti 5Si 3Compoundization improved the fracture toughness of material; In addition, the research paper that is published in " Journal of theEuropean Ceramic Society, 2002,22:551-558 " shows that percent by volume is 14~35 TiC and Ti 5Si 3Composite is increased to~4.2MPam from 3.0 with its fracture toughness of increase of in-situ ceramic mark 1/2Ceramic particle TiB 2Be suitable as very much Ti because of having high-melting-point, high rigidity, low-density and good excellent properties such as thermal conductivity 5Si 3The enhancing body.Regrettably, relevant TiB 2Pottery strengthens Ti 5Si 3Research few.
Combustion synthesis reaction is that the fuel factor of utilizing reactant generation chemical reaction process to discharge is kept reaction voluntarily, thus synthetic new thing phase.Combustion synthesis reaction has that technology is easy, equipment is simple, energy consumption is low, aggregate velocity is exceedingly fast and advantage such as low pollutions, is widely used in high-temperature materials such as the ceramic and intermetallic compound of preparation.Because TiB 2Pottery and Ti 5Si 3The forming process of intermetallic compound all belongs to high exothermic heat of reaction, and therefore, combustion synthesis technology is highly suitable for TiB 2Pottery strengthens Ti 5Si 3The preparation of intermetallic compound composite material.
Summary of the invention
The purpose of this invention is to provide that a kind of technology is easy, equipment is simple, energy consumption is low, and the original position TiB that is easy to apply 2-Ti 5Si 3Composite and preparation method thereof.
Technical scheme of the present invention is: under the protection of high-purity argon gas, the reactant pressed compact of a certain proportion of B powder, Si powder and Ti powder is placed on carries out combustion synthesis reaction in the combustion and synthesis device.After reaction finished, it is densified that the reactant pressed compact is pressurizeed, and prepares original position TiB 2Pottery strengthens Ti 5Si 3Intermetallic compound composite material.Specific embodiment comprises that the preparation of reactant pressed compact and reaction form original position TiB 2Pottery strengthens Ti 5Si 3Two stages of intermetallic compound composite material:
1) reactant pressed compact preparation:
A. the reactant pressed compact is formed: be made up of less than 44 microns B powder, Si powder and Ti powder powder particles, wherein the percentage by weight of B powder is 0.3≤B≤6.2, and the percentage by weight of Si powder is 20.8≤Si≤25.8, and all the other are the Ti powder;
B. batch mixing: take by weighing powder according to aforementioned proportion, and batch mixing 6 ± 1 hours in the ball mill of packing into, make it to mix;
C. compression moulding: the powder that mixes is put into mould, compression moulding at room temperature, and the pressed compact compact rate of molding is 70 ± 6%;
2) reaction forms original position TiB 2-Ti 5Si 3Composite:
A. preheating: the reactant pressed compact is placed in the combustion and synthesis device, vacuumizes back 1 atmospheric high-purity argon gas of feeding and protect, with resistance wire the reactant pressed compact is heated to 450~600 degree and carries out preheating, and be incubated 20~25 minutes;
B. combustion synthesis reaction: continue to utilize resistance heat that the reactant pressed compact is heated, combustion synthesis reaction takes place until it; Perhaps the arc heat that produces with tungsten electrode in reactant pressed compact bottom is lighted, and causes combustion synthesis reaction;
C. densified: after combustion synthesis reaction finishes, the reactant pressed compact is applied the pressure of 15~30 MPas, and pressurize 5~20 minutes, make it densified, form original position TiB 2Pottery strengthens Ti 5Si 3Intermetallic compound composite material.
The present invention compares with present existing technology has following characteristics:
The original position TiB that the invention provides a kind of simple and reliable process, saves the energy and be easy to apply 2Pottery strengthens Ti 5Si 3Intermetallic compound composite material and preparation method thereof;
1) adopts B powder, Si powder and Ti powder as reactant system, form TiB by the chemical reaction original position 2Pottery and Ti 5Si 3Intermetallic compound;
2) original position TiB 2Pottery strengthens Ti 5Si 3TiB in the intermetallic compound composite material 2And Ti 5Si 3Be metallurgical binding, the interface is clean, in conjunction with good.
3) the heat heating systems that utilizes reactant generation chemical reaction to discharge is saved the energy, the efficient height.
The specific embodiment
Embodiment one
(1) B powder, Si powder and the Ti powder of powder particles less than 44 microns taken by weighing in the ratio shown in the table 1, and batch mixing 6 ± 1 hours in the ball mill of packing into, make it to mix; Then powder is put into mould, at room temperature be pressed into base, the pressed compact compact rate of molding is 70 ± 6%;
(2) the reactant pressed compact is placed in the combustion and synthesis device, vacuumizes back 1 atmospheric high-purity argon gas of feeding and protect, with resistance wire the reactant pressed compact is heated to 450~600 degree and carries out preheating, and be incubated 20~25 minutes;
(3) continue to utilize resistance heat to the heating of reactant pressed compact, combustion synthesis reaction takes place until it;
(4) after combustion synthesis reaction finishes, the reactant pressed compact is applied the pressure of 15~30 MPas, and pressurize 5~20 minutes, make it densified, thereby form original position TiB 2Pottery strengthens Ti 5Si 3Intermetallic compound composite material.Original position TiB 2Pottery strengthens Ti 5Si 3Intermetallic compound composite material and Ti 5Si 3The intermetallic compound base body is compared, and hardness has improved 22~30%, and fracture toughness has improved 2~4 times.
Table 1 reactant preparation of powder ratio
Figure GSA00000029214900031
Embodiment two
(1) B powder, Si powder and the Ti powder of powder particles less than 44 microns taken by weighing in the ratio shown in the table 2, and batch mixing 6 ± 1 hours in the ball mill of packing into, make it to mix; Then powder is put into mould, at room temperature be pressed into base, the pressed compact compact rate of molding is 70 ± 6%;
(2) the reactant pressed compact is placed in the combustion and synthesis device, vacuumizes back 1 atmospheric high-purity argon gas of feeding and protect, with resistance wire the reactant pressed compact is heated to 450~600 degree and carries out preheating, and be incubated 20~25 minutes;
(3) light with the arc heat that tungsten electrode produces reactant pressed compact bottom, causes combustion synthesis reaction;
(4) after combustion synthesis reaction finishes, the reactant pressed compact is applied the pressure of 15~30 MPas, and pressurize 5~20 minutes, make it densified, thereby form original position TiB 2Pottery strengthens Ti 5Si 3Intermetallic compound composite material.
Table 2 reactant preparation of powder ratio
Figure GSA00000029214900032

Claims (4)

1. original position TiB 2-Ti 5Si 3Composite is characterized in that, TiB in the composite 2The percentage by weight of pottery is 1≤TiB 2≤ 20, all the other are Ti 5Si 3Intermetallic compound, and TiB 2Pottery is to form Ti by Ti powder and B powder by the chemical reaction original position 5Si 3Intermetallic compound is to form TiB by chemical reaction by Ti powder and Si powder 2And Ti 5Si 3Between be metallurgical binding.
2. a kind of original position TiB according to claim 1 2-Ti 5Si 3Composite is characterized in that described TiB 2The best in quality percentage of ceramic particle is 3≤TiB 2≤ 10.
3. a kind of original position TiB according to claim 1 2-Ti 5Si 3Composite is characterized in that, described TiB 2Pottery is an in-situ particle, and it is of a size of submicron order, is shaped as hexa-prism.
4. one kind is used for the described a kind of original position TiB of claim 1 2-Ti 5Si 3The preparation method of composite is characterized in that, the preparation process of this composite may further comprise the steps:
1) reactant pressed compact preparation:
A. the reactant pressed compact is formed: be made up of less than 44 microns B powder, Si powder and Ti powder powder particles, wherein the percentage by weight of B powder is 0.3≤B≤6.2, and the percentage by weight of Si powder is 20.8≤Si≤25.8, and all the other are the Ti powder;
B. batch mixing: take by weighing powder according to aforementioned proportion, and batch mixing 6 ± 1 hours in the ball mill of packing into, make it to mix;
C. compression moulding: the powder that mixes is put into mould, compression moulding at room temperature, and the pressed compact compact rate of molding is 70 ± 6%;
2) reaction forms original position TiB 2-Ti 5Si 3Composite:
A. preheating: the reactant pressed compact is placed in the combustion and synthesis device, vacuumizes back 1 atmospheric high-purity argon gas of feeding and protect, with resistance wire the reactant pressed compact is heated to 450~600 degree and carries out preheating, and be incubated 20~25 minutes;
B. combustion synthesis reaction: continue to utilize resistance heat that the reactant pressed compact is heated, combustion synthesis reaction takes place until it; Perhaps the arc heat that produces with tungsten electrode in reactant pressed compact bottom is lighted, and causes combustion synthesis reaction;
C. densified: after combustion synthesis reaction finishes, the reactant pressed compact is applied the pressure of 15~30 MPas, and pressurize 5~20 minutes, make it densified, form original position TiB 2Pottery strengthens Ti 5Si 3Intermetallic compound composite material.
CN2010191000120A 2010-02-08 2010-02-08 In-situ TiB2 and Ti5Si3 composite material and preparation method thereof Active CN101811190B (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN2010191000120A CN101811190B (en) 2010-02-08 2010-02-08 In-situ TiB2 and Ti5Si3 composite material and preparation method thereof

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN2010191000120A CN101811190B (en) 2010-02-08 2010-02-08 In-situ TiB2 and Ti5Si3 composite material and preparation method thereof

Publications (2)

Publication Number Publication Date
CN101811190A CN101811190A (en) 2010-08-25
CN101811190B true CN101811190B (en) 2011-12-21

Family

ID=42618634

Family Applications (1)

Application Number Title Priority Date Filing Date
CN2010191000120A Active CN101811190B (en) 2010-02-08 2010-02-08 In-situ TiB2 and Ti5Si3 composite material and preparation method thereof

Country Status (1)

Country Link
CN (1) CN101811190B (en)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN102211939A (en) * 2011-05-19 2011-10-12 哈尔滨工程大学 ZrO2 enhanced Ti5Si3 composite material and preparation method thereof
CN109295336B (en) * 2018-12-12 2020-10-20 中国科学院兰州化学物理研究所 Preparation method of titanium-silicon alloy phase reinforced TiAl-based composite material with network structure

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4915903A (en) * 1984-10-19 1990-04-10 Martin Marietta Corporation Process for forming composites having an intermetallic containing matrix
CN1933869A (en) * 2004-03-29 2007-03-21 法伊鲁特株式会社 Ring with health promoting capability

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4915903A (en) * 1984-10-19 1990-04-10 Martin Marietta Corporation Process for forming composites having an intermetallic containing matrix
CN1933869A (en) * 2004-03-29 2007-03-21 法伊鲁特株式会社 Ring with health promoting capability

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
周卫兵.Synthesis of Ti_3SiC_2/TiB_2 Composite by In-situ Hot Pressing (HP) Method.《Journal of Wuhan University of Technology(Materials Science Edition)》.2008,(第06期), *

Also Published As

Publication number Publication date
CN101811190A (en) 2010-08-25

Similar Documents

Publication Publication Date Title
CN104073674B (en) A kind of preparation method of Graphene aluminum matrix composite
CN102219536B (en) B4C/SiC whisker/SiC multiphase ceramic matrix composite and preparation method thereof
CN101486588B (en) Preparation of carbon fiber reinforced carbon-silicon carbide double matrix friction material
CN101456737B (en) Boron carbide base composite ceramic and preparation method thereof
Xu et al. Combustion synthesis and densification of titanium diboride–copper matrix composite
CN104045350B (en) Method for preparing silicon nitride /silicon carbide ceramic composite by use of reaction sintering process
CN107162597A (en) A kind of formula of moulding by casting silicon nitride products based on silicon carbide and preparation method thereof
CN112125315B (en) Low-cost high-purity silicon hexaboride production process
CN102515770B (en) Method for preparing nano SiC reinforced MoSi2 composite material
CN113233899A (en) B4B4C-SiC-Si composite material generated by siliconizing reaction of C/graphite preform and preparation method thereof
CN101798222A (en) Al2O3-Ni-C-B4C composite ceramic and preparation method thereof
CN101811190B (en) In-situ TiB2 and Ti5Si3 composite material and preparation method thereof
CN103938006A (en) Manufacturing method of cermet material resistant to molten aluminum corrosion
CN103553619A (en) Titanium carbide and vanadium carbide composite material as well as production method and application thereof
JP5356991B2 (en) Method for producing titanium silicon carbide ceramics
CN101812622A (en) Ceramic-intermetallic compound composite material containing binder and preparation method thereof
CN101734920A (en) Titanium nitride porous ceramics and preparation method thereof
JP5308296B2 (en) Method for producing titanium silicon carbide ceramics
Fielding et al. Gas-cooled fast reactor fuel fabrication
CN101486564B (en) Preparation of boron nitride nano tube enhanced alumina ceramic
JP2002285258A (en) Metal-ceramic composite material and production method therefor
CN103938051B (en) The preparation method of the corrosion of resistance to aluminium high desnity metal ceramic material
CN103938050B (en) The corrosion of resistance to aluminium high desnity metal stupalith
CN102249697A (en) Method for promoting sintering of titanium boride ceramic by using reaction aids
Akhlaghi et al. Role of Ti3AlC2 MAX phase on characteristics of in-situ synthesized TiAl intermetallics. Part IV: mechanical properties

Legal Events

Date Code Title Description
C06 Publication
PB01 Publication
SE01 Entry into force of request for substantive examination
C14 Grant of patent or utility model
GR01 Patent grant