CN100554457C - The method of self-spreading high-temperature synthesis of TiCo porous material - Google Patents

The method of self-spreading high-temperature synthesis of TiCo porous material Download PDF

Info

Publication number
CN100554457C
CN100554457C CNB200710118212XA CN200710118212A CN100554457C CN 100554457 C CN100554457 C CN 100554457C CN B200710118212X A CNB200710118212X A CN B200710118212XA CN 200710118212 A CN200710118212 A CN 200710118212A CN 100554457 C CN100554457 C CN 100554457C
Authority
CN
China
Prior art keywords
self
powder
tico
high temperature
temperature
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.)
Expired - Fee Related
Application number
CNB200710118212XA
Other languages
Chinese (zh)
Other versions
CN101078067A (en
Inventor
郝俊杰
吴玉博
郭志猛
罗骥
李艳
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.)
University of Science and Technology Beijing USTB
Original Assignee
University of Science and Technology Beijing USTB
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 University of Science and Technology Beijing USTB filed Critical University of Science and Technology Beijing USTB
Priority to CNB200710118212XA priority Critical patent/CN100554457C/en
Publication of CN101078067A publication Critical patent/CN101078067A/en
Application granted granted Critical
Publication of CN100554457C publication Critical patent/CN100554457C/en
Expired - Fee Related legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Images

Abstract

A kind of method of self-spreading high-temperature synthesis of TiCo porous material belongs to powder metallurgy-self propagating high temperature synthesis technical field.With titanium valve and drillings is raw material, mixes the back and adopts the method for powder compression to prepare base substrate, and base substrate one end is connected with the W silk of portfire, puts into the vacuum reaction synthesizer, and vacuum tightness is higher than 4 * 10 -2Begin during Pa to heat up, reach starting ignition device after the temperature of preheating, the self propagating high temperature building-up reactions promptly takes place, obtain the self propagating high temperature synthetic sample.Advantage is: prepared TiCo alloy porosity is 30-55%, and percentage of open area is more than 50%, and ultimate compression strength is at 100-377MPa, and Young's modulus is at 8-40GPa, and Young's modulus and its mechanical property can be adjusted by the size of porosity fully.

Description

The method of self-spreading high-temperature synthesis of TiCo porous material
Technical field
The invention belongs to powder metallurgy-self propagating high temperature synthesis technical field, a kind of method of self-spreading high-temperature synthesis of TiCo porous material is provided especially, powder pressing forming-self propagating high temperature synthetic (Self-propagatingHigh-temperature Synthesis, abbreviation SHS) TiCo alloy porous material.
Background technology
Self propagating high temperature synthesizes (SHS), is to utilize chemical reaction self heat release to prepare the new technology of material.SHS is a kind of material new synthetic method that is grown up by USSR (Union of Soviet Socialist Republics) the sixties in 20th century, its outstanding feature is exactly the high energy thermopositive reaction that makes full use of when forming compound between element, except causing the necessary a small amount of external energy of building-up reactions, entire reaction course mainly relies on the heat release of material self to keep.Therefore, this technology can be saved resource greatly, and this technology also has synthetic technology short, and the product purity height is low in the pollution of the environment, the logging material synthetic be sintered in outstanding advantage such as one.
The TiCo alloy is as a kind of titanium alloy material, has that intensity height, proportion are low, antifatigue, corrosion-resistant, wear-resistant, low magnetic, an advantage such as nontoxic; Simultaneously, the TiCo alloy also has good biocompatibility, especially porous TiCo alloy is easy to be fixed by human body, and because its good three-dimensional communication hole, can make the tissue metabolism of human body, the transmission of nutritive substance in human body is uncrossed to be carried out, so TiCo alloy porous material is a kind of highly desirable permanent implantation medical material, has broad application prospects in medical field.
The rarely seen in the world report of development of present porous TiCo alloy.Domestic research focuses mostly on the basis of TiCo dense material, its technological process adopts the mode of LASER HEAT spraying to plate one deck to several layers of TiCo alloy layer on the titanium matrix, make pure titanium material not only have superior corrosion resistance energy, abrasion resistance properties but also mechanical property and also improve greatly, therefore obtained concern to a certain degree at home.But fine and close TiCo alloy material is owing to the mechanical property of mechanical property considerably beyond the bone of human body, joint material, its Young's modulus (100GPa) is higher than the stress shielding that human body bone, joint material (1-40GPa) cause embedded material and matrix easily far away, cause material loosening, cause the graft failure of material.
Porous TiCo alloy material, both brought into play that good corrosion-resistant, the rub resistance of this alloy, low magnetic, proportion are low, performances such as antifatigue and excellent biological compatibility, again by introducing three-dimensional porous structure, improved the mechanical compatibility of itself and human body bone, joint material, make its Young's modulus reach the degree that is complementary with human body bone, joint, so this material will become the research focus of biological stephanoporate medical material.It is better that practical application mesoporosity degree is controlled at 30-70%, and prepared material should present isotropic hole connectedness, and bore hole size distributes and is mainly 50-500 μ m.
Powder pressing forming is a kind of technology of preparation powdered material of widespread usage.This processing unit is simple, and the working hour is short, and therefore flexible and convenient operation adopts this moulding process, helps reducing production cost, for the industrialization process of product provides a great convenience.
Summary of the invention
The object of the present invention is to provide a kind of method of self-spreading high-temperature synthesis of TiCo porous material, because porous material adopts the method for adding pore-forming material more at present, though porosity can reach more than 50%, the intensity extreme difference can not use as the biological substitution material.Self propagating high temperature sintering resultant is a kind of intermetallic compound, have very high intensity, and the heat in the reaction process is enough to the deposite metal element, hole in the pressed compact is kept and is interconnected.Solved between the intensity of present bio-medical material and the porosity can not matched well problem.
Adopt granularity 2-300 μ mTi powder and 2-300 μ mCo powder as starting material, 40%-60% takes by weighing raw material powder according to the Ti atomic percent, and ball milling mixes.On hydraulic dynamometer, adopt 100MPa-400MPa pressure cold stamping die molded.Base substrate is placed in the vacuum reaction synthesizer, vacuumizes.Treat that vacuum tightness reaches 1 * 10 -2-4 * 10 -2Begin behind the Pa to heat up, the preheating temperature scope is 100-600 ℃, reach preheating temperature after, the self propagating high temperature building-up reactions with the tungsten filament base substrate that ignites, can take place in insulation 10-30min starting ignition device, obtains the self propagating high temperature sintered products.
The invention has the advantages that: prepared TiCo alloy porous material porosity is 30-55%, percentage of open area can reach more than 50%, bore hole size is at 50-500 μ m, can satisfy that general osseous tissue is grown into and the transmission of human physiological activity, meta-bolites is carried out smoothly.The synthetic porous TiCo of institute alloy compressive strength is between 85-377MPa, and folding strength is between 50-280MPa, and Young's modulus is at 8-20GPa, is close with the Young's modulus of the netted osseous tissue of human body, can satisfy the requirement of strength of bone.
Description of drawings:
0 ℃ of preheating 10min of Figure 145, sample SEM photo.
00 ℃ of preheating 10min of Figure 25, sample SEM photo.
Embodiment
Embodiment 1
Adopt 20 μ mTi powder and 2 μ mCo powder as starting material, according to 1: 1 ball mill mixing of atomic ratio.
This mixed powder 6g that weighs with scale puts into cylindrical mold compression molding under 100MPa.
Base substrate is packed in the self-control vacuum reaction synthesizer, and base substrate one end contacts with the W silk of portfire, and forvacuum reaches 4 * 10 -2Pa begins to heat up then, and preheating temperature is 450 ℃, is incubated starting ignition device after 10 minutes, by the W silk blank that ignites, the self propagating high temperature building-up reactions can take place, and obtains the self propagating high temperature sintered sample.
The porosity of planting the TiCo alloy porous insert of prepared thus is 40.5%, and percentage of open area is 40%, and the ultimate compression strength during compression is 323Mpa, and the Young's modulus of material is 9.0Gpa.
The stereoscan photograph of the TiCo alloy porous insert of this kind prepared is seen Fig. 1
Case study on implementation 2
Its working method and processing condition are substantially with case study on implementation one, unique different be that preheating temperature before the self propagating high temperature building-up reactions takes place is 500 ℃.
It is 30.9% that the porosity of the TiCo alloy porous insert of this prepared is arranged, and percentage of open area is 70.4%; Ultimate compression strength during compression is 334Mpa, and folding strength is that Young's modulus is 11.0Gpa.
TiCo alloy porous insert stereoscan photograph such as Fig. 2 of this prepared.

Claims (1)

1, the method for self-spreading high-temperature synthesis of TiCo porous material is characterized in that: adopt Ti powder and Co powder as starting material, 40%-60% takes by weighing raw material powder according to the Ti atomic percent, and ball mill mixing makes material mixing even; Under hydraulic dynamometer, use 100-400MPa pressure cold stamping die molded; The base substrate that suppresses is placed the vacuum reaction synthesizer, vacuumize; Treat that vacuum tightness reaches 1 * 10 -2-4 * 10 -2Pa begins to heat up, and the preheating temperature scope is 100-600 ℃, reach preheating temperature after, insulation 10min-30min, the self propagating high temperature building-up reactions with the tungsten filament base substrate that ignites, takes place this moment in the starting ignition device; The question response container is cooled to room temperature, obtains the self propagating high temperature sintered products; The granularity of Ti powder is 2-300 μ m; The granularity of Co powder is 2-300 μ m.
CNB200710118212XA 2007-07-02 2007-07-02 The method of self-spreading high-temperature synthesis of TiCo porous material Expired - Fee Related CN100554457C (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CNB200710118212XA CN100554457C (en) 2007-07-02 2007-07-02 The method of self-spreading high-temperature synthesis of TiCo porous material

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CNB200710118212XA CN100554457C (en) 2007-07-02 2007-07-02 The method of self-spreading high-temperature synthesis of TiCo porous material

Publications (2)

Publication Number Publication Date
CN101078067A CN101078067A (en) 2007-11-28
CN100554457C true CN100554457C (en) 2009-10-28

Family

ID=38905730

Family Applications (1)

Application Number Title Priority Date Filing Date
CNB200710118212XA Expired - Fee Related CN100554457C (en) 2007-07-02 2007-07-02 The method of self-spreading high-temperature synthesis of TiCo porous material

Country Status (1)

Country Link
CN (1) CN100554457C (en)

Families Citing this family (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CA2851250A1 (en) 2011-10-05 2013-04-11 Texas Tech University Antibacterial metallic nanofoam and related methods
CN103205721B (en) * 2013-03-19 2015-10-28 昆山海普电子材料有限公司 A kind of production method of titanium-aluminium alloy target material
CN103182507B (en) * 2013-03-19 2015-04-15 昆山海普电子材料有限公司 Production method of chromium-aluminium alloy target material
CN104532058B (en) * 2014-12-15 2017-02-22 中南大学 Medical implanted porous cobalt-titanium alloy material and preparation method thereof
CN104588660B (en) * 2015-01-07 2016-12-07 中南大学 A kind of solid phase combustion synthetic method preparing porous metals integral section
CN105695800A (en) * 2016-04-14 2016-06-22 熊启兵 Bracket for power grid
CN106448792B (en) * 2016-10-11 2018-08-31 西南科技大学 A kind of preparation method of aspidelite type prosthetic graft
US20180281055A1 (en) * 2017-03-29 2018-10-04 The Boeing Company Titanium-Cobalt Alloy And Associated Thixoforming Method
CN109161725A (en) * 2018-09-10 2019-01-08 江苏大学 A kind of preparation method of the Ti-24Nb-4Zr-7.9Sn alloy of Co alloying
CN110041075B (en) * 2019-05-21 2021-05-28 哈尔滨师范大学 Rapid preparation method of high-purity Nb2SnC ceramic powder
CN113957279B (en) * 2021-10-27 2022-04-26 东北大学 Explosion-proof method and device for self-propagating production of kilogram-grade gamma-TiAlNb alloy in one-step furnace

Non-Patent Citations (4)

* Cited by examiner, † Cited by third party
Title
自蔓延高温合成(SHS)及其应用(二). 杨遇春.稀有金属,第6期. 1991
自蔓延高温合成(SHS)及其应用(二). 杨遇春.稀有金属,第6期. 1991 *
自蔓延高温合成的材料和工艺. 汪华林等.功能材料,第27卷第3期. 1996
自蔓延高温合成的材料和工艺. 汪华林等.功能材料,第27卷第3期. 1996 *

Also Published As

Publication number Publication date
CN101078067A (en) 2007-11-28

Similar Documents

Publication Publication Date Title
CN100554457C (en) The method of self-spreading high-temperature synthesis of TiCo porous material
CN106552940B (en) A kind of preparation method of the ordered porous TiAg alloys of gradient
CN101956091B (en) Method for preparing titanium alloy material through gelcasting-selfpropagation high-temperature synthesis
CN103060589B (en) Preparation method of gradient nickel (Ni) titanium (Ti) shape-memory alloy with multiple pores
CN102534284A (en) Method for preparing medical porous NiTi shape memory alloy by microwave sintering
CN101948964A (en) Method for preparing biomedical porous titanium and titanium alloy material
WO2013037094A1 (en) Light-weight gradient cemented carbide sealing ring and method for manufacturing same
CN106513681A (en) Preparation method of graded porous nickel-titanium alloy
CN107115825A (en) A kind of Gem Grade large single crystal diamond Multicarity composite structure and its preparation method and application
WO2011011606A3 (en) Methods of forming sintered boron carbide
CN103266319A (en) Method for preparing porous titanium coating on surface of titanium alloy
Juneja et al. Development of Corn Starch-Neusilin UFL2 conjugate as tablet superdisintegrant: Formulation and evaluation of fast disintegrating tablets
CN106007684A (en) Graphene alumina ceramic composite material and preparation method thereof
CN101255060B (en) Method for preparing diffusion couple by using powder
CN102303977A (en) Method for preparing titanium-iron particle reinforced hydroxyapatite-based bioceramic material
CN104491923A (en) Nanometer/micrometer-crystal gradient structure calcium phosphate bio-ceramic material as well as preparation method and application thereof
CN104998301A (en) Preparation method of carbon nano tube reinforced mesoporous hydroxyapatite composite material
CN103205589B (en) Hard alloy taking Ni-Al intermetallic compound as binding phase and preparation method thereof
CN110744059A (en) Medical porous low-modulus titanium-magnesium alloy and forming method and application thereof
CN102251138B (en) Preparation method of nickel titanium foam alloy with double pore structure
CN109534385B (en) Nano-pore-rich silver sulfide and rapid preparation method thereof
CN102220508B (en) Preparation method and usage of medical porous tantalum
CN108165811A (en) A kind of preparation method of high-strength degradable nanometer medical porous titanium magnesium base composite material
CN205326393U (en) Novel boracic diamond compact piece of interface growth type
CN104532058A (en) Medical implanted porous cobalt-titanium alloy material and preparation 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
C14 Grant of patent or utility model
GR01 Patent grant
C17 Cessation of patent right
CF01 Termination of patent right due to non-payment of annual fee

Granted publication date: 20091028

Termination date: 20120702