CN1382660A - Composite Ti-HA material and its preparing process - Google Patents
Composite Ti-HA material and its preparing process Download PDFInfo
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- CN1382660A CN1382660A CN 02124091 CN02124091A CN1382660A CN 1382660 A CN1382660 A CN 1382660A CN 02124091 CN02124091 CN 02124091 CN 02124091 A CN02124091 A CN 02124091A CN 1382660 A CN1382660 A CN 1382660A
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- powder
- water glass
- matrix material
- sintering
- baking
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- 238000000034 method Methods 0.000 title description 7
- 239000000463 material Substances 0.000 title description 5
- 239000002131 composite material Substances 0.000 title 1
- 238000005245 sintering Methods 0.000 claims abstract description 23
- 239000000843 powder Substances 0.000 claims abstract description 21
- 235000019353 potassium silicate Nutrition 0.000 claims abstract description 20
- NTHWMYGWWRZVTN-UHFFFAOYSA-N sodium silicate Chemical compound [Na+].[Na+].[O-][Si]([O-])=O NTHWMYGWWRZVTN-UHFFFAOYSA-N 0.000 claims abstract description 20
- 239000011159 matrix material Substances 0.000 claims description 17
- 238000007599 discharging Methods 0.000 claims description 8
- 238000009413 insulation Methods 0.000 claims description 7
- 239000011812 mixed powder Substances 0.000 claims description 7
- 238000002360 preparation method Methods 0.000 claims description 5
- 239000000203 mixture Substances 0.000 abstract description 12
- 238000002156 mixing Methods 0.000 abstract description 6
- 239000003795 chemical substances by application Substances 0.000 abstract 1
- 238000010438 heat treatment Methods 0.000 abstract 1
- 239000010936 titanium Substances 0.000 description 35
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 6
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 6
- 229910052588 hydroxylapatite Inorganic materials 0.000 description 6
- XYJRXVWERLGGKC-UHFFFAOYSA-D pentacalcium;hydroxide;triphosphate Chemical compound [OH-].[Ca+2].[Ca+2].[Ca+2].[Ca+2].[Ca+2].[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O XYJRXVWERLGGKC-UHFFFAOYSA-D 0.000 description 6
- 229910002804 graphite Inorganic materials 0.000 description 5
- 239000010439 graphite Substances 0.000 description 5
- 238000011056 performance test Methods 0.000 description 5
- 229910052719 titanium Inorganic materials 0.000 description 5
- 238000010792 warming Methods 0.000 description 5
- 238000005303 weighing Methods 0.000 description 5
- 206010018910 Haemolysis Diseases 0.000 description 4
- 230000008588 hemolysis Effects 0.000 description 4
- 229910001069 Ti alloy Inorganic materials 0.000 description 2
- 210000001124 body fluid Anatomy 0.000 description 2
- 239000010839 body fluid Substances 0.000 description 2
- 210000000988 bone and bone Anatomy 0.000 description 2
- 239000011248 coating agent Substances 0.000 description 2
- 238000000576 coating method Methods 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- 230000007797 corrosion Effects 0.000 description 2
- 238000005260 corrosion Methods 0.000 description 2
- 238000005516 engineering process Methods 0.000 description 2
- 239000007943 implant Substances 0.000 description 2
- 238000002791 soaking Methods 0.000 description 2
- 210000001519 tissue Anatomy 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- 229910014497 Ca10(PO4)6(OH)2 Inorganic materials 0.000 description 1
- 241000372132 Hydrometridae Species 0.000 description 1
- 230000004071 biological effect Effects 0.000 description 1
- 239000000316 bone substitute Substances 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 238000001514 detection method Methods 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- 229910021645 metal ion Inorganic materials 0.000 description 1
- 239000007769 metal material Substances 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 238000007750 plasma spraying Methods 0.000 description 1
- 238000004826 seaming Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 230000007704 transition Effects 0.000 description 1
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- Materials For Medical Uses (AREA)
Abstract
A Ti/HA composition is prepared from HA (48-78 wt.%), Ti (18-48 wt.%) and water glass as passivating agent (4-5 wt.%) through mixing HA powder with Ti powder while adding water glass, baking, loading in mould, putting in plasma discharge sintering furnace, vacuumizing, pressurizing to 20-30 MPa, heating to 800-950 deg.C at speed of 80-150 deg.C/min, and holding the temp for 2-10 min. Its advantages are high strnegth and compactness, and having bioactivity.
Description
Technical field
A kind of Ti/HA matrix material and preparation method thereof belongs to the sintering technology field.
Background technology
Titanium or titanium alloy because in light weight, intensity is high, has certain biocompatibility again, the main raw of being implanted and repairing as bone by people always.Yet, behind the metallic substance implant into body, cause the metallic surface corrosion even make metal ion enter when injected organism tissue making when injected organism tissue rotten owing in the body fluid environment, being on active service for a long time.A kind of method that addresses this problem is that modification is carried out in the metallic surface, generate one deck biologically active can with human body synosteosis surface of good.Hydroxyapatite (Ca
10(PO
4)
6(OH)
2Hereinafter to be referred as HA), be the main component of human body bone, be a kind of good bone substitute.What employing was more at present is in matrix Ti surface plasma spraying HA coating, yet Ti and HA belong to nonwettable two kinds of materials mutually, so the interface between coating and matrix belongs to typical mechanical bond.Clinically show that with behind the above-mentioned materials implant into body, body fluid easily is penetrated at the interface along the slit of mechanical bond, causes the interfacial corrosion disbonding, thereby to improve bonding strength should be preferred plan to obtain metallurgical bonding interface.The another kind of method that addresses the above problem is that directly that HA and Ti is powder sintered, microcosmic is compound.Owing to adopt the form of gradient transition can realize that intensity combines with active, but adopt the higher sintering temperature of this kind method needs, and be difficult to take into account simultaneously HA and Ti does not react and macroscopical sintering.
Summary of the invention
Problem to be solved by this invention is to overcome the problem that exists in the aforesaid method, and a kind of intensity height is provided, and compactness is good, biologically active, and realized Ti/HA matrix material of metallurgical binding between Ti and the HA and preparation method thereof.
Ti/HA matrix material provided by the present invention is characterized in that: contain the HA that weight percent is 48-78%, the Ti of 18-48%, the water glass of 4-5%.
The preparation method of Ti/HA matrix material provided by the present invention is characterized in that, it may further comprise the steps: (1) adds water glass as passivator when HA powder and Ti powder are mixed, baking; (2) with above-mentioned three kinds of mixed powder dress moulds, carry out sintering in discharging plasma sintering equipment, vacuumize, pressurization 20～30MPa is to be rapidly heated 800-950 ℃ under the 80-150 ℃/min in speed, insulation 2-10min.
The present invention has added a certain amount of water glass as passivator, the reaction when having avoided sintering between Ti and the HA on the prescription of material.The present invention has adopted the sintering method of plasma discharging, under special sintering mechanism.Low temperature, Fast Sintering has realized not decomposing of HA, and has obtained metallurgical binding, has the intensity height, compactness is good, the Ti/HA matrix material of biologically active.
From Fig. 2,3 Photomicrograph as can be seen, add water glass passivator after, hole significantly reduces, sintering is fine and close more, has realized between Ti and the HA well metallurgical binding.
See Table 1, sintered specimen is soaked in water measure its pH value after 7 days: pH value reacts when changing the explanation sintering, has novel substance to generate; PH value does not react generation when not changing the explanation sintering.Corresponding variation biocompatibility along with PH also changes.
Detecting percentage of hemolysis is an integral part of Bioexperiment, can the detection of biological activity, and be the requisite index that material is used for biological direction, be less than or equal to 5 for qualified.
The water glass passivator of Ti/HA adding 4% carries out sintering among the embodiment 1, compare as seen with Comparative Examples, its hardness has improved 26%, relative density has improved 24.7 percentage points, after in water, soaking, the solution pH value no longer changes, and percentage of hemolysis reaches 4, satisfies clinical requirement (percentage of hemolysis should be less than or equal to 5).
Description of drawings
Fig. 1: agglomerating mould synoptic diagram.
The Photomicrograph of Fig. 2: Ti/HA (1: 1) matrix material.
Fig. 3: Ti/HA (1: 1) adds the Photomicrograph of water glass (4%) back matrix material.
F is an applied pressure among Fig. 1; 1. mould seaming chuck, 2. carbon paper, 3. mixed powder, 4. die coat, 5. mould push-down head.
Embodiment
1. get hydroxylapatite powder 4.8g, titanium valve 4.8g and water glass 0.4g join powder, put into mixed powder machine and mix, and after mixing, baking is 1 hour in 100 ℃ of baking ovens.Taking by weighing above-mentioned powder mix 4g then packs in the graphite jig of φ 24, compacting, put into discharging plasma sintering equipment, be evacuated to 4Pa, plus-pressure 30MPa, 100 ℃/min of heat-up rate, be warming up to 870 ℃ of insulation 3min, slowly cool to room temperature and take out, obtain the Ti/HA matrix material, its performance test sees Table 1.
2. get hydroxylapatite powder 5.95g, titanium valve 3.55g and water glass 0.5g join powder, put into mixed powder machine and mix, and after mixing, baking is 1 hour in 100 ℃ of baking ovens.Taking by weighing above-mentioned powder mix 4g then packs in the graphite jig of φ 24, compacting, put into discharging plasma sintering equipment, be evacuated to 4Pa, plus-pressure 30MPa, 100 ℃/min of heat-up rate, be warming up to 870 ℃ of insulation 3min, slowly cool to room temperature and take out, obtain the Ti/HA matrix material, its performance test sees Table 1.
3. get hydroxylapatite powder 7.8g, titanium valve 1.8g and water glass 0.4g join powder, put into mixed powder machine and mix, and after mixing, baking is 1 hour in 100 ℃ of baking ovens.Taking by weighing above-mentioned powder mix 4g then packs in the graphite jig of φ 24, compacting, put into discharging plasma sintering equipment, be evacuated to 4Pa, plus-pressure 30MPa, 100 ℃/min of heat-up rate, be warming up to 870 ℃ of insulation 3min, slowly cool to room temperature and take out, obtain the Ti/HA matrix material, its performance test sees Table 1.
4. get hydroxylapatite powder 7.8g, titanium valve 1.8g and water glass 0.4g mix, and after mixing, baking is 1 hour in 100 ℃ of baking ovens.Taking by weighing above-mentioned powder mix 4g then packs in the graphite jig of φ 24, compacting, put into discharging plasma sintering equipment, be evacuated to 4Pa, plus-pressure 20MPa, 80 ℃/min of heat-up rate, be warming up to 850 ℃ of insulation 2min, slowly cool to room temperature and take out, obtain the Ti/HA matrix material, its performance test sees Table 1.
5. get hydroxylapatite powder 7.8g, titanium valve 1.8g and water glass 0.4g join powder, put into mixed powder machine and mix, and after mixing, baking is 1 hour in 100 ℃ of baking ovens.Taking by weighing above-mentioned powder mix 4g then packs in the graphite jig of φ 24, compacting, put into discharging plasma sintering equipment, be evacuated to 4Pa, plus-pressure 30MPa, 100 ℃/min of heat-up rate, be warming up to 870 ℃ of insulation 3min, slowly cool to room temperature and take out, obtain the Ti/HA matrix material, its performance test sees Table 1.
Table 1
| Composition (weight percent) | Sintering process | Hardness (HRA) | Density (g/cm 3) | Relative density (%) | Sintered specimen soaks the pH value after 7 days in water | Percentage of hemolysis (%) | ||||
| Pressure (MPa) | Heat-up rate (℃/min) | Sintering temperature (℃) | Soaking time (min) | |||||||
| Comparative Examples | ???Ti∶HA(50∶50) | ????30 | ????100 | ??870 | ????3 | ????47 | ????2.63 | ????69.7 | ????13 | ????30 |
| | Ti: HA: water glass (48: 48: 4) | ????30 | ????100 | ??870 | ????3 | ????60 | ????3.57 | ????94.4 | ????7 | ????4 |
| Embodiment 2 | Ti: HA: water glass (35.5: 59.5: 5) | ????30 | ????100 | ??870 | ????3 | ????54 | ????3.45 | ????95.8 | ????7 | ????4 |
| Embodiment 3 | Ti: HA: water glass (18: 78: 4) | ????30 | ????100 | ??870 | ????3 | ????50 | ????3.27 | ????99.1 | ????7 | ????3 |
| Embodiment 4 | Ti: HA: water glass (18: 78: 4) | ????20 | ????80 | ??850 | ????2 | ????46 | ????3.21 | ????97.3 | ????7 | ????3 |
| | Ti: HA: water glass (18: 78: 4) | ????30 | ????150 | ??950 | ????10 | ????52 | ????3.28 | ????99.4 | ????7 | ????3 |
Claims (2)
1, a kind of Ti/HA matrix material is characterized in that: contain the HA that weight percent is 48-78%, the Ti of 18-48%, the water glass of 4-5%.
2, the preparation method of Ti/HA matrix material according to claim 1 is characterized in that, it may further comprise the steps: (1) adds water glass as passivator when HA powder and Ti powder are mixed, baking; (2) with above-mentioned three kinds of mixed powder dress moulds, carry out sintering in discharging plasma sintering equipment, vacuumize, pressurization 20～30MPa is warmed up to 800-950 ℃ under 80-150 ℃/min, insulation 2-10min.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CNB021240914A CN1169746C (en) | 2002-06-19 | 2002-06-19 | Composite Ti-HA material and its preparing process |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CNB021240914A CN1169746C (en) | 2002-06-19 | 2002-06-19 | Composite Ti-HA material and its preparing process |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CN1382660A true CN1382660A (en) | 2002-12-04 |
| CN1169746C CN1169746C (en) | 2004-10-06 |
Family
ID=4745325
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CNB021240914A Expired - Fee Related CN1169746C (en) | 2002-06-19 | 2002-06-19 | Composite Ti-HA material and its preparing process |
Country Status (1)
| Country | Link |
|---|---|
| CN (1) | CN1169746C (en) |
Cited By (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN1296321C (en) * | 2003-12-15 | 2007-01-24 | 中国科学院金属研究所 | Process for sintering ceramic powder or ceramic base composite powder |
| CN1304195C (en) * | 2004-12-14 | 2007-03-14 | 清华大学 | Micelle ceramic/metal block composite material and preparation method thereof |
| CN104353120A (en) * | 2014-11-10 | 2015-02-18 | 苏州蔻美新材料有限公司 | Method for preparing polymethacrylate/hydroxyapatite composite biological ceramic material |
| CN104353119A (en) * | 2014-11-10 | 2015-02-18 | 苏州蔻美新材料有限公司 | Method for preparing polyglycolic acid/hydroxyapatite composite biological ceramic material |
| CN104383593A (en) * | 2014-11-10 | 2015-03-04 | 苏州蔻美新材料有限公司 | Preparation method of polycaprolactone/hydroxyapatite composite biological ceramic material |
| CN104436296A (en) * | 2014-11-10 | 2015-03-25 | 苏州蔻美新材料有限公司 | Preparation method of polylactic/hydroxyapatite composite biological ceramic material |
| CN104941003A (en) * | 2015-06-10 | 2015-09-30 | 中南大学 | Titanium/tricalcium phosphate composite applied to bone implanting material and preparation method of titanium/tricalcium phosphate composite |
| CN110201222A (en) * | 2019-07-05 | 2019-09-06 | 中南大学 | One kind facilitating bone titanium containing rubidium tantalum composite material and preparation method and application |
-
2002
- 2002-06-19 CN CNB021240914A patent/CN1169746C/en not_active Expired - Fee Related
Cited By (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN1296321C (en) * | 2003-12-15 | 2007-01-24 | 中国科学院金属研究所 | Process for sintering ceramic powder or ceramic base composite powder |
| CN1304195C (en) * | 2004-12-14 | 2007-03-14 | 清华大学 | Micelle ceramic/metal block composite material and preparation method thereof |
| CN104353120A (en) * | 2014-11-10 | 2015-02-18 | 苏州蔻美新材料有限公司 | Method for preparing polymethacrylate/hydroxyapatite composite biological ceramic material |
| CN104353119A (en) * | 2014-11-10 | 2015-02-18 | 苏州蔻美新材料有限公司 | Method for preparing polyglycolic acid/hydroxyapatite composite biological ceramic material |
| CN104383593A (en) * | 2014-11-10 | 2015-03-04 | 苏州蔻美新材料有限公司 | Preparation method of polycaprolactone/hydroxyapatite composite biological ceramic material |
| CN104436296A (en) * | 2014-11-10 | 2015-03-25 | 苏州蔻美新材料有限公司 | Preparation method of polylactic/hydroxyapatite composite biological ceramic material |
| CN104941003A (en) * | 2015-06-10 | 2015-09-30 | 中南大学 | Titanium/tricalcium phosphate composite applied to bone implanting material and preparation method of titanium/tricalcium phosphate composite |
| CN110201222A (en) * | 2019-07-05 | 2019-09-06 | 中南大学 | One kind facilitating bone titanium containing rubidium tantalum composite material and preparation method and application |
| CN110201222B (en) * | 2019-07-05 | 2021-09-07 | 中南大学 | Composite material for promoting bone to contain rubidium, titanium and tantalum and preparation method and application thereof |
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| Publication number | Publication date |
|---|---|
| CN1169746C (en) | 2004-10-06 |
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