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 PDFInfo
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- 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
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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
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
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
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.
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CN101811190B true CN101811190B (en) | 2011-12-21 |
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Families Citing this family (2)
Publication number | Priority date | Publication date | Assignee | Title |
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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)
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 |
-
2010
- 2010-02-08 CN CN2010191000120A patent/CN101811190B/en active Active
Patent Citations (2)
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)
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), * |
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