JPS5945976A - Apatite-titanium complex material and manufacture - Google Patents
Apatite-titanium complex material and manufactureInfo
- Publication number
- JPS5945976A JPS5945976A JP57154035A JP15403582A JPS5945976A JP S5945976 A JPS5945976 A JP S5945976A JP 57154035 A JP57154035 A JP 57154035A JP 15403582 A JP15403582 A JP 15403582A JP S5945976 A JPS5945976 A JP S5945976A
- Authority
- JP
- Japan
- Prior art keywords
- apatite
- powder
- avatai
- sintering
- titanium
- 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
Links
Landscapes
- Compositions Of Oxide Ceramics (AREA)
- Dental Preparations (AREA)
- Dental Prosthetics (AREA)
Abstract
(57)【要約】本公報は電子出願前の出願データであるた
め要約のデータは記録されません。(57) [Summary] This bulletin contains application data before electronic filing, so abstract data is not recorded.
Description
【発明の詳細な説明】
本発明は、医用インブラン1〜月どし’C38りるアパ
タイト−チタン系複合月利J5よびその製造法に関Jる
。DETAILED DESCRIPTION OF THE INVENTION The present invention relates to apatite-titanium composite J5 for medical use, and a method for producing the same.
従来、例えば南II用<Kどに用いるインブラン]・材
としては、生体に24 ?Jる親和性の而からアパタイ
ト系セラミックが優れていることが明らかにされている
が、強位F」η性71<劣る点て・実用面でtl1点が
ある。一方、金属は強度面では(縁れているbのの中に
はaj性のあるものもあり、市111のへい金属ても牛
イホに対りる親和性のIj、!(゛は待に期待できるb
の【、Lない。Conventionally, for example, Inblan used for South II <K> and materials used for living organisms are 24? It has been revealed that apatite ceramics are superior in terms of their affinity for J, but they have a strong F'η property of 71<inferior points and a tl1 point in practical terms. On the other hand, in terms of strength, metals (some of the edged b's have aj characteristics, and even the metals of city 111 have an affinity for cow iho! can be expected b
[, L not.
アルミリ系JrA利は1′!クミツクどしくは強目的に
優れており、生体に対18毒性もない安定な材料どして
最近ン1目されでいるが、靭性の点では前記アパタイト
系1ごラミックとl1j1様にヒラミックの域を出るは
どの物11Iを示してい(’Lい。Aluminum JrA profit is 1'! Kumitsuku has excellent strength and has recently been attracting attention as a stable material with no toxicity to living organisms, but in terms of toughness, it is in the level of the apatite type 1, lamic, and l1j1. Exit shows which object 11I ('L).
そこで、本発明では、アパタイト系〔ビラミックの牛体
に対り゛る親和1![/!r利用し、これに金属′vi
利のもつ靭性をト1加して、その欠点をカバーし、イン
ブラン1〜月として有用な口利を提供ぜんどするもので
ある。Therefore, in the present invention, apatite-based [Biramic's affinity for bovine body] 1! [/! r, and metal 'vi
By adding the toughness of the steel, it makes up for its shortcomings and provides a useful advantage as an in-bran.
すなわち、本発明第1項の発明はアパタイトあるいはざ
らに石英を加えた二すのをバイ副ガラス系フリッ)・ど
ともに焼結してなる焼結セラミック体に、チタンあるい
はさらにアバタイ1〜を添加1ノで焼結してなる焼結金
属月別を複合一体化してなることを特徴どりるアパタイ
ト−チタン系複合材料を要旨どづるものである。That is, the invention of item 1 of the present invention is a sintered ceramic body formed by sintering apatite or quartz and a bi-sub-glass type frit. This article outlines an apatite-titanium composite material that is characterized by being made by integrating sintered metals that are sintered in one step.
十−記焼結ヒラミック体におGプるアバターr1・(ま
、前述のように焼結体としてインブラン1〜月に適した
ものであるが、これに石英粉末を加えるど、膨張と焼成
収縮の調節効果がある。又、焼結金属4.J illに
お(〕るチタンは軽量で靭111に冨み、かつ毒性もな
く、焼結セラミック体と複合一体化I!シめることにJ
、す、焼結セラミック体の前記欠点を補完しインブラン
ト材どしく優れたものとなる、。Avatar r1 (well, as mentioned above, it is suitable as a sintered body for 1 to 1 month), but when quartz powder is added to it, it expands and shrinks during firing. In addition, titanium, which is used in sintered metals, is lightweight, has a high toughness of 111, and is non-toxic. J
, it compensates for the drawbacks of the sintered ceramic body and becomes an excellent implant material.
第2項の発明は、アバタイ1−粉末!i(>−100%
、石英粉末0・〜・50%にバー(Aガラス系フリッ1
〜粉末を外削で1〜15%添加してなるセラミック月利
と、”r t If < $5)末50 ヘ−75%、
Ti金属粉末25・〜・50%にアバタイ1〜粉末を外
削で0〜5%添加しくなる金属口利とを複合せしめ、不
活i’JI M tri真空雰囲気(−1200・〜、
1300°Cで焼結覆ることを特徴とりるアバターr+
・−チタン系複合+411の製造法を背旨とザるもので
ある。The invention of item 2 is Avatai 1-Powder! i(>-100%
, quartz powder 0...50% bar (A glass frit 1
~Ceramic yield made by adding 1 to 15% of powder by external grinding, and "r t If < $5) end of 50 to 75%,
By combining the Ti metal powder 25 to 50% with a metal advantage that makes it possible to add 0 to 5% of Avatai 1 to powder by external machining, it is possible to create an inert i'JI M tri vacuum atmosphere (-1200 to 50%).
Avatar r+ is characterized by being sintered at 1300°C.
- This is based on the manufacturing method of titanium-based composite +411.
この第2項の発明(こお(]るl′!ラミック月利に用
いるアパタイトどh矢わ)末の/11東覧ま前述のとお
りCあるが、石英粉末の50%以1.の添加はアバタイ
1〜の効果を減殺りるので好ましクイ【い。The invention of Section 2 (hereinafter referred to as "Apatite used for lamic monthly production") is the last part of the 11th edition of the invention. is preferable because it reduces the effect of Avatai 1~.
まlご、セラミック月利の焼結助剤どして、バイオガラ
ス系フリットをハ1いるが、これは1200〜1300
T;’で・焼結さけるための助剤ど【ノ(の効果があり
、か゛つ、゛j′バタイI・どf−1矢□どの焼結11
、ケに(1月〕る親11目りと接合手Δ判の生体に対J
−る親和性の白土効果を秦Jるものである。Actually, bio-glass frit is used as a sintering aid for ceramics, but it costs 1,200 to 1,300 yen.
There is an effect of auxiliary agent to avoid sintering in T;
, against the biological body of the parent 11 eyes and the joint Δ size in January (January)
- This is the result of the Shirato effect of affinity.
バイオガラスとは、生1本親和11.1の良好なガラス
で本弁明に用いるにりT適なものを例示りるど、S!0
220.O〜40.0%、八λ2030 〜5.0%、
B20j 35.(lへ、 45.0%、l” 20
h4.0〜20.0%、C,a Q 1.0 〜9.0
%、Na 2 ()IO・〜15.0% 4する絹成例
の−6のがある。かかるバイオガラスは1000〜14
00℃で溶融し、フリッ]・化して用いる。Bioglass is a glass with a good glass affinity of 11.1 and is suitable for use in this defense. 0
220. O~40.0%, 8λ2030~5.0%,
B20j 35. (To l, 45.0%, l” 20
h4.0-20.0%, C, a Q 1.0-9.0
%, Na2()IO・~15.0% There is a -6 silk example with 4%. Such bioglass is 1000-14
It is melted at 00°C and used as a frit.
このバイA万うス系フリツ1−は 1%末)口1ではそ
の効果がなく、15%を越える添加はアパタイトの効果
を減殺するとともに、1200〜− 1300°Cでの
焼結時に軟化、変形、発泡りるので好ましくない。This Bi-A million-based frit 1- (1% powder) has no effect, and addition of more than 15% reduces the effect of apatite and softens during sintering at 1200 to -1300°C. This is not preferable because it causes deformation and foaming.
一1記ヒラミック(A料は上記組成の範囲内で第1図に
示1如ぎ膨張率と第2図に示1”如き収縮率並びに曲げ
強電を示ず。11 Hiramic (A material) does not exhibit an expansion rate as shown in FIG. 1 as shown in FIG. 1, a shrinkage rate as shown in FIG. 2 as shown in FIG.
本発明の金属材料におけるTiH4粉末は焼成時に収縮
して焼成収縮率を調inl する効果があり、又、アパ
タイト粉末は焼結体の膨111率を調1Mlす°る効果
がある。−1−ill4は!)()%未満では焼結金属
月利が焼結セラミック体よりも収縮率が人きく /にり
過さ゛てθfましくlr<、7h%を越えると、収縮率
が焼結セラミック(A利J:りも小さく/、1り過ぎで
′りYましくない1.1パタイト粉末は5%を越えると
、金属材わ1の11!j I’l 、狛1J靭竹を到1
害し−Cり「11ノクイ多゛い。The TiH4 powder in the metal material of the present invention has the effect of shrinking during firing and adjusting the firing shrinkage rate, and the apatite powder has the effect of adjusting the expansion rate of the sintered body by 1Ml. -1-ill4 is! )()%, the shrinkage rate of the sintered metal monthly rate is more impressive than that of the sintered ceramic body. 1.1 Patite powder exceeds 5%, and metal material 1 of 11!j
Damage-C: ``11 times too many.''
かかる金属+A Flの焼結体(j、1−記絹成の範囲
内で第3図に示J如ン\;慮服ヰと第4図(J示C」如
ぎ収縮率並びに曲げ強電を小り、。Such a sintered body of metal + A Fl (j, 1- within the range of the silk formation as shown in Figure 3) and Figure 4 (J shown C) has a shrinkage rate and a strong bending electric current. Small.
1−記しラミック月a:qど金属(A利どは、例えば第
5図に示したように、ブ1ノス成形などにより金属月利
1を二1アどし、しラミック+A $312を外殻層と
する複合汁粉成形体とする。両材料は前記第1〜4図に
シiζした116月11v・収縮率に阜づいで、それぞ
れの伯がなるべく一致Jるように組成を選定づる。1 - Marked lamic month a: q metal (A rate is, for example, as shown in Fig. 5, add metal monthly rate 1 to 21 by bu 1 nos molding etc. and remove lamic + A $312. A composite powder molded body is used as a shell layer.The compositions of both materials are selected based on the shrinkage rates shown in Figs.
n粉成形体は不?1Ii1!l :li(は貞空Jり囲
気中で焼結する。すなわら、不活性雰囲気の場合は)フ
ルボンガス気流中で、又、内空雰囲気の揚台(よ10
’ 1−orr以下で、1200−.1300’CF焼
結号−る。このifb+ Iαα四囲、ブタンの焼結)
品1αが1200−・140 (1℃、一方、)′バク
イトの焼結渦電が1100〜1300°Cであることか
ら、両者の焼結編1α範囲である1200〜1300℃
を採ったものである。不活性又は真空雰囲気でlf <
、例えば酸素弁1’Eの存在ド(・はチタンが酸化づ
°るので好ましくない。n Is the powder molded product not acceptable? 1Ii1! 1: Li (sintering is carried out in an empty atmosphere, i.e., in the case of an inert atmosphere) in a fulbone gas stream, or on a lifting platform in an internal atmosphere.
' 1-orr or less, 1200-. 1300'CF sintered number. This ifb+ Iαα4, butane sintering)
Product 1α is 1200-・140 (1℃, on the other hand)' Since the sintering eddy current of Bakite is 1100-1300℃, the sintering 1α range of both products is 1200-1300℃.
It was taken from In an inert or vacuum atmosphere lf <
For example, the presence of the oxygen valve 1'E is not preferable because titanium will be oxidized.
本発明にJ、れば、コアは金属化し、外殻は焼結ヒラミ
ック化した二層構造をなした複合体が得られる。そして
、ヒラミックと金1+Aどは膨III係数がほぼ等しく
その界面には20〜3071mのチタン酸化物にりなる
中間層が形成され、両層の結合が強固になっている。According to the present invention, a composite having a two-layer structure in which the core is metallized and the outer shell is sintered and ceramic is obtained. The expansion III coefficients of Hiramic and gold 1+A are almost equal, and an intermediate layer of titanium oxide with a thickness of 20 to 3071 m is formed at the interface, and the bond between the two layers is strong.
外殻にアパタイト系セラミックを使うことで生体親和性
に優れ、又、コアにチタンを用いることにJ、り軽tl
!で高強度な物Y′iが1シIられ、医用インブランI
−材どじて有用な材わ1どなる。The use of apatite ceramic for the outer shell has excellent biocompatibility, and the use of titanium for the core makes it extremely
! A high-strength material Y′i was added to the medical inductor I
- The wood is so useful that it roars.
又、粉末焼結法によるので形状は自由にJることができ
る利点知ある。Also, since it is based on the powder sintering method, it has the advantage that the shape can be freely shaped.
つぎに実施例についで説明りる。Next, examples will be explained.
下記表に示した組成に、に V)A、132種の8利を
用意した。、表中の中位は重fi1%である。V) A, 132 types of 8 compounds were prepared in the composition shown in the table below. , the middle level in the table is heavy fi1%.
表
△ [3
二l T ! l−14$5)末
!−+ 0 6 (
1ア Ti1Il屈粉末 50 40月 アバ
タイ1〜粉
末(外削)10
例 アバタI’l−粉末 70 60イー1 英
わ)未 3 0
4 0殻 フリッI・(外削)53
外殻に用いるフリットは Na co 3:St ’0
2 : (Ea III〕o4 @ 21120
:Ca CO3: Na 2 ()・l”32051
0t120−2 : 3: 2: 1: 2(
中ω比)の乾式)17合物を1 (l O0℃で溶融フ
リット化しI、:ものである。Table △ [3 2l T! l-14$5) end
! −+ 0 6 (
1A Ti1Il-powder 50 40 months Avatai 1~Powder (external cutting) 10 Example Avata I'l-powder 70 60E1 English
W) Not yet 30
4 0 shell Frit I・(Outer cutting) 53 The frit used for the outer shell is Na co 3:St '0
2: (Ea III] o4 @ 21120
:Ca CO3: Na 2 ()・l”32051
0t120-2: 3: 2: 1: 2(
The dry method) 17 compound with medium ω ratio) was melted and fritted at 0°C to give I.
A、13とt)にアクリル系バイングを用い−(造粒し
、乾式)゛レスで第5)図に示す如き二層構造体の圧!
5)体を成形し2だ1.つい(゛、これらを12 !+
(1°(’、 ’C:]′ルfンカス中(・焼成しl
こ。A, 13 and t) using acrylic buying - (granulated and dry) 5) Pressure of the two-layer structure as shown in Figure!
5) Mold the body 2.1. Just (゛, these are 12!+
(1°(', 'C:]' during firing)
child.
その結果、]アは金属化し、外殻は焼結セラミック化(
)Iこ一ニ層)f/> 3Kjの複合体が1!ノられた
。]アと外殻どの界面は20〜30 Ilmのチタン酸
化物層を中間層どしく強固/r結合と<’L・)(いI
こ。As a result, ]a becomes metallized, and the outer shell becomes sintered ceramic (
) I this one layer) f/> 3Kj complex is 1! I was beaten. ] The interface between A and the outer shell is a titanium oxide layer of 20 to 30 Ilm with strong /r bonding and <'L・)(I
child.
上記は不活性雰囲気−C焼結しlご例を示したが、真空
中で焼結しても同様の1)のが得られた。Although the above example shows the case of inert atmosphere-C sintering, the same example 1) was also obtained by sintering in vacuum.
第1図は本発明に用いる【ヒ′)ミック+4利の膨n艮
率を示づグラフ、第2図は同収縮率と強度を示タグラフ
、Wl 3図は本発明1、“用いる金属H料の膨張率を
示Jグラノ、第4図は同収縮率ど強電を示り゛グラフ、
第5図は実施例の成形体の一例を示J斜視図で゛ある。
1・・・・・・=11 2・・・・・・外殻1ηh′[
出願人 鳴jlti製陶株式会社代理人弁理ト 小 松
秀 畠Figure 1 is a graph showing the expansion ratio of [hy')mic+4 ratio used in the present invention, Figure 2 is a graph showing the shrinkage rate and strength, Figure 4 shows the expansion rate of the material and the graph shows the contraction rate.
FIG. 5 is a perspective view showing an example of the molded product of the embodiment. 1...=11 2...Outer shell 1ηh'[
Applicant Ningjlti Ceramic Co., Ltd. Attorney Hide Komatsu Hatake
Claims (2)
のをバイ副ガラス系フリッ1−どどもに焼結してなる焼
結セラミック体に、チタンあるいはさらにアパタイトを
添加して焼結してなる焼結金属材料を複合一体化してな
ることを特徴どりるアバタイ!〜−ヂタン系枚合+A
$A 。(1) A sintered ceramic body made by adding quartz to a sintered ceramic body and sintering it together with titanium or apatite. Avatai is characterized by being made of composite metal materials! ~-Ditane series + A
$A.
下同じ)、6英粉末0〜50%にパイΔカラス系フリッ
1〜粉末を外削で1〜15%添加してなるセラミック+
J l’31ど、−r f Ll 4粉末50〜75%
、−[1金属粉末25〜50%にアバタイ1〜粉末を外
削′cθ〜5%添加してなる金属材料とを複合せしめ、
不活性又は貞空雰囲気で1200〜1300℃で焼l1
llcJ−ることを特徴とJるアパタイト−チタン系複
合材料の製造法。(2) Ceramic + made by adding 1 to 15% of PiΔ Karasu-based Furi 1 to 50 to 100% (1!, the same applies hereinafter) of Avatai 1 powder and 0 to 50% of 6 powder by external machining.
J l'31, -r f Ll 4 powder 50-75%
, - Composite a metal material obtained by adding 25 to 50% of Avatai 1 to 50% of Avatai 1 to 5% of outer cutting 'cθ,
Baked at 1200-1300℃ in an inert or clean atmosphere
llcJ- A method for producing an apatite-titanium composite material.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP57154035A JPS5945976A (en) | 1982-09-06 | 1982-09-06 | Apatite-titanium complex material and manufacture |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP57154035A JPS5945976A (en) | 1982-09-06 | 1982-09-06 | Apatite-titanium complex material and manufacture |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS5945976A true JPS5945976A (en) | 1984-03-15 |
| JPS6140623B2 JPS6140623B2 (en) | 1986-09-10 |
Family
ID=15575481
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP57154035A Granted JPS5945976A (en) | 1982-09-06 | 1982-09-06 | Apatite-titanium complex material and manufacture |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS5945976A (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS62132756A (en) * | 1985-12-04 | 1987-06-16 | 株式会社アドバンス | High strength calcium phosphate base ceramic material |
-
1982
- 1982-09-06 JP JP57154035A patent/JPS5945976A/en active Granted
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS62132756A (en) * | 1985-12-04 | 1987-06-16 | 株式会社アドバンス | High strength calcium phosphate base ceramic material |
Also Published As
| Publication number | Publication date |
|---|---|
| JPS6140623B2 (en) | 1986-09-10 |
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